Drugs / Capecitabine
last change yesterday re-read 8 days ago

Capecitabine

English name capecitabine

Small molecule targets TYMS

Developed for
colorectal cancer · breast cancer · gastric cancer · rectal cancer · malignant pancreatic neoplasm · nasopharyngeal carcinoma · gastric adenocarcinoma · gastroesophageal junction adenocarcinoma
+207 more · triple-negative breast carcinoma · pancreatic adenocarcinoma · cancer · esophageal cancer · HER2 positive breast carcinoma · rectal carcinoma · biliary tract cancer · rectum adenocarcinoma · cancer of unknown primary site · female breast carcinoma · metastatic malignant neoplasm · hepatocellular carcinoma · colon carcinoma · gastroesophageal adenocarcinoma · metastatic neoplasm · colorectal carcinoma · metastasis from malignant tumor of colon · rectal neoplasm · neoplasm · colorectal neoplasm · gastroesophageal cancer · esophageal squamous cell carcinoma · Her2-receptor negative breast cancer · pancreatic ductal adenocarcinoma · cholangiocarcinoma · esophageal adenocarcinoma · gastric neoplasm · head and neck cancer · colorectal adenocarcinoma · digestive system cancer · gallbladder cancer · metastatic malignant neoplasm in the brain · non-small cell lung carcinoma · adenocarcinoma · estrogen-receptor positive breast cancer · gastric carcinoma · hormone receptor-positive breast cancer · intrahepatic cholangiocarcinoma · colon adenocarcinoma · head and neck squamous cell carcinoma · neuroendocrine neoplasm · peritoneal carcinomatosis · carcinoma · extrahepatic bile duct carcinoma · gallbladder carcinoma · hilar cholangiocarcinoma · invasive breast carcinoma · ovarian cancer · pancreatic neoplasm · pancreatic neuroendocrine tumor · renal cell carcinoma · anal canal squamous cell carcinoma · breast neoplasm · cervical cancer · digestive system neoplasm · liver cancer · male breast carcinoma · malignant colon neoplasm · prostate cancer · bile duct cancer · bile duct carcinoma · carcinoma of esophagus · central nervous system cancer · digestive system neuroendocrine neoplasm · glucagonoma · head and neck neoplasm · hypopharynx squamous cell carcinoma · neoplastic meningitis · neuroendocrine carcinoma · oropharynx squamous cell carcinoma · pancreas disorder · pancreatic endocrine carcinoma · pancreatic insulinoma · peritoneum cancer · skin squamous cell carcinoma · small intestine adenocarcinoma · somatostatinoma · adult hepatocellular carcinoma · anal carcinoma · anal margin squamous cell carcinoma · anal squamous cell carcinoma · anus basaloid carcinoma · appendix carcinoma · carcinoma of gallbladder and extrahepatic biliary tract · cloacogenic carcinoma · colonic disorder · colonic neoplasm · cutaneous neuroendocrine carcinoma · digestive system carcinoma · distal biliary tract carcinoma · endometrial cancer · fallopian tube cancer · gastrin-producing neuroendocrine tumor · glioblastoma · high grade malignant neoplasm · hypopharyngeal carcinoma · inflammatory breast carcinoma · kidney cancer · laryngeal squamous cell carcinoma · malignant leptomeningeal tumor · nasal cavity and paranasal sinus squamous cell carcinoma · oral cavity cancer · ovarian carcinoma · ovarian mucinous cystadenocarcinoma · pancreatic exocrine neoplasm · PPoma · progesterone-receptor positive breast cancer · pseudomyxoma peritonei · refractory malignant neoplasm · squamous cell carcinoma · thyroid cancer · adrenal cortex carcinoma · adult glioblastoma · ampulla of vater adenocarcinoma · anal canal cancer · biliary tract neoplasm · bone cancer · bone neoplasm · brain glioma · brain stem glioma · BRCA1-related cancer predisposition · BRCA2-related cancer predisposition · breast carcinoma · carcinoid tumor · central nervous system disorder · central nervous system neoplasm · cervical adenosquamous carcinoma · childhood malignant neoplasm · clear cell adenocarcinoma · clear cell renal carcinoma · combined hepatocellular carcinoma and cholangiocarcinoma · diffuse gastric adenocarcinoma · ductal breast carcinoma in situ and lobular carcinoma in situ · endocrine gland neoplasm · Epstein-Barr virus-related tumor · estrogen-receptor negative breast cancer · exocrine pancreatic carcinoma · fallopian tube carcinoma · female reproductive organ cancer · gallbladder adenocarcinoma · gastric cardia carcinoma · gastric intestinal type adenocarcinoma · gastric linitis plastica · gastric neuroendocrine neoplasm · glioma · intestinal neuroendocrine neoplasm · intraepithelial neoplasia · invasive lobular breast carcinoma · kidney neoplasm · larynx cancer · larynx verrucous carcinoma · lip and oral cavity squamous cell carcinoma · liver and intrahepatic bile duct neoplasm · lung neuroendocrine neoplasm · male reproductive organ cancer · malignant adrenal gland pheochromocytoma · malignant endocrine neoplasm · malignant glioma · malignant mesothelioma · malignant soft tissue neoplasm · malignant urinary system neoplasm · medullary thyroid gland carcinoma · metastatic carcinoma · metastatic malignant neoplasm in the colon · metastatic malignant neoplasm in the lymph nodes · multiple endocrine neoplasia type 1 · multiple endocrine neoplasia type 2A · multiple endocrine neoplasia type 2B · nasopharyngeal neoplasm · neoplasm of esophagus · non-functional pancreatic neuroendocrine tumor · non-Hodgkin lymphoma · oral cavity squamous cell carcinoma · ovarian germ cell tumor · pancreatic acinar cell carcinoma · pancreatic intraductal papillary-mucinous neoplasm · pancreatic large cell neuroendocrine carcinoma · pancreatic neuroendocrine neoplasm · paranasal sinus squamous cell carcinoma · periampullary adenocarcinoma · peritoneal carcinoma · pharynx cancer · pituitary gland adenoma · progesterone-receptor negative breast cancer · prostate carcinoma · renal cell adenocarcinoma · respiratory system cancer · salivary gland squamous cell carcinoma · secondary malignant neoplasm · skin cancer · small intestine cancer · small intestine neuroendocrine tumor, well differentiated, low or intermediate grade · soft tissue sarcoma · thrombotic thrombocytopenic purpura · thymic neuroendocrine tumor · urothelial carcinoma · uterine adnexa cancer · vaginal cancer · verrucous carcinoma of oral cavity · VIPoma · Zollinger-Ellison syndrome · anus neoplasm · bile duct neoplasm · brain cancer · breast carcinoma by gene expression profile · extrahepatic bile duct adenocarcinoma · malignant exocrine pancreas neoplasm
Investigated by
National Cancer Institute (NCI) · Hoffmann-La Roche · Fudan University · Sun Yat-sen University · Sanofi · Roche Pharma AG
+880 more · Genentech, Inc. · Cancer Institute and Hospital, Chinese Academy of Medical Sciences · Alliance for Clinical Trials in Oncology · M.D. Anderson Cancer Center · Pfizer · Zhejiang Cancer Hospital · Bristol-Myers Squibb · Henan Cancer Hospital · ImmunityBio, Inc. · Tianjin Medical University Cancer Institute and Hospital · Eli Lilly and Company · Shanghai Zhongshan Hospital · Asan Medical Center · Chinese Academy of Medical Sciences · GlaxoSmithKline · Peking University Cancer Hospital & Institute · Ruijin Hospital · AstraZeneca · Dana-Farber Cancer Institute · Novartis Pharmaceuticals · Roswell Park Cancer Institute · Fujian Cancer Hospital · Merck Sharp & Dohme LLC · Peking Union Medical College Hospital · The First Affiliated Hospital with Nanjing Medical University · UNICANCER · West China Hospital · Massachusetts General Hospital · Memorial Sloan Kettering Cancer Center · SWOG Cancer Research Network · Zhejiang University · GBG Forschungs GmbH · Liaoning Cancer Hospital & Institute · Peking University · Royal Marsden NHS Foundation Trust · Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins · Brigham and Women's Hospital · H. Lee Moffitt Cancer Center and Research Institute · Harbin Medical University · Hebei Medical University Fourth Hospital · Jiangsu HengRui Medicine Co., Ltd. · National Cancer Center, Korea · Sanofi-Synthelabo · Second Affiliated Hospital, School of Medicine, Zhejiang University · Stanford University · University Hospital of Crete · University of Washington · Hellenic Oncology Research Group · Nanfang Hospital, Southern Medical University · National Cancer Centre, Singapore · Novartis · The Netherlands Cancer Institute · Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · University of Michigan Rogel Cancer Center · University of Southern California · Beth Israel Deaconess Medical Center · Celgene Corporation · Chia Tai Tianqing Pharmaceutical Group Co., Ltd. · City of Hope Medical Center · European Organisation for Research and Treatment of Cancer - EORTC · Georgetown University · NRG Oncology · NSABP Foundation Inc · Seoul National University Hospital · Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University · Swiss Cancer Institute · Tongji Hospital · Bayer · Beijing Friendship Hospital · Cancer Research UK · Columbia University · Eisai Inc. · Federation Francophone de Cancerologie Digestive · First Affiliated Hospital of Zhejiang University · all 886 on the full record

Regulatory milestones approvals, filings & regulatory actions · 8 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Label expansions (6) US (FDA) XELODA — 2001-04-30 – 2022-12-14 fda.gov ↗
Approved EU (EMA) Xeloda — 2001-02-02 europa.eu ↗
Approved US (FDA) XELODA — 1998-04-30 fda.gov ↗

Trials 1,521 · started per year

today
US approved 1998
EU approved 2001
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1998199920002001200220032004200520062007200820092010201120122013201420152016201720182019202020212022202320242025202620272028
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 04 trials
Phase 0 NCT06406816 May 2024 → May 2026 overdue intrahepatic cholangiocarcinoma Yongyi Zeng Recruiting No outcome recorded
Phase 0 NCT05238831 Jan 2023 → May 2026 female breast carcinoma, ovarian carcinoma, pancreatic ductal adenocarcinoma, pancreatic large cell neuroendocrine carcinoma +2 OHSU Knight Cancer Institute Withdrawn No outcome recorded
Phase 0 NCT03515941 Jun 2018 → Mar 2020 digestive system cancer Tannaz Armaghany Terminated No outcome recorded
Phase 0 NCT01821612 May 2013 → Nov 2014 pancreatic acinar cell carcinoma, pancreatic ductal adenocarcinoma Alliance for Clinical Trials in Oncology Completed No outcome recorded
Phase 1169 trials · 2 met primary
Phase 1 NCT07824934 Sep 2026 → May 2028 expected cancer Sunshine Lake Pharma Co., Ltd. Recruiting No outcome recorded
Phase 1 NCT07453875 May 2026 → Nov 2027 expected peritoneal carcinomatosis Daping Hospital and the Research Institute of Surgery of the Third Military Medical University Not yet recruiting No outcome recorded
Phase 1 NCT07477743 Mar 2026 → Dec 2027 expected — HC Biopharma Inc. Recruiting No outcome recorded
Phase 1 NCT05296005 Dec 2025 gastric adenocarcinoma, gastroesophageal junction adenocarcinoma Ohio State University Comprehensive Cancer Center Withdrawn No outcome recorded
Phase 1 NCT06848465 Feb 2025 → Aug 2026 overdue metastasis from malignant tumor of colon Daping Hospital and the Research Institute of Surgery of the Third Military Medical University Recruiting No outcome recorded
Phase 1 NCT06621563 Dec 2024 → Mar 2026 overdue colorectal cancer, non-small cell lung carcinoma Hansoh BioMedical R&D Company Recruiting No outcome recorded
Phase 1 NCT06065371 Nov 2024 → Dec 2026 expected digestive system cancer Henry Ford Health System Recruiting No outcome recorded
Phase 1 NCT06544655 Oct 2024 → Oct 2027 expected cancer Bristol-Myers Squibb Active not recruiting No outcome recorded
Phase 1 NCT06825624 Oct 2024 → Oct 2026 expected colorectal cancer Hansoh BioMedical R&D Company Recruiting No outcome recorded
Phase 1 NCT06346808 May 2024 → May 2026 overdue malignant pancreatic neoplasm Sichuan University Not yet recruiting No outcome recorded
Show all 169 trials opens the full record — a long page
Phase 1/2143 trials · 5 met primary · 1 missed
Phase 1/2 NCT07791758 Sep 2026 → Sep 2030 expected colorectal carcinoma Nanjing Leads Biolabs Co.,Ltd Not yet recruiting No outcome recorded
Phase 1/2 NCT07653685 Sep 2026 → Jun 2027 expected colorectal cancer Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd. Recruiting No outcome recorded
Phase 1/2 NCT07805551 Aug 2026 → Aug 2030 expected colorectal cancer Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd. Recruiting No outcome recorded
Phase 1/2 NCT07681297 Aug 2026 → Aug 2028 expected central nervous system disorder, triple-negative breast carcinoma National University Hospital, Singapore Not yet recruiting No outcome recorded
Phase 1/2 NCT07494448 Jul 2026 → Dec 2027 expected HER2 positive breast carcinoma MedSIR Not yet recruiting No outcome recorded
Phase 1/2 NCT07683949 Jun 2026 → Oct 2029 expected colorectal cancer Seoul National University Bundang Hospital Enrolling by invitation No outcome recorded
Phase 1/2 NCT07327229 Feb 2026 → Sep 2027 expected gastroesophageal adenocarcinoma Antengene Biologics Limited Recruiting No outcome recorded
Phase 1/2 NCT07140393 Oct 2025 → Oct 2027 expected neoplasm Jiangsu HengRui Medicine Co., Ltd. Recruiting No outcome recorded
Phase 1/2 NCT07161791 Sep 2025 → Dec 2026 expected triple-negative breast carcinoma Harbin Medical University Not yet recruiting No outcome recorded
Phase 1/2 NCT06942234 Jun 2025 → Jun 2027 expected Her2-receptor negative breast cancer Jiangsu Alphamab Biopharmaceuticals Co., Ltd Recruiting No outcome recorded
Show all 143 trials opens the full record — a long page
Phase 2865 trials · 26 met primary · 29 missed
Phase 2 NCT07841873 Nov 2026 → Jun 2028 expected biliary tract cancer Anhui Provincial Hospital Not yet recruiting No outcome recorded
Phase 2 NCT07797244 Oct 2026 → Apr 2029 expected colorectal cancer Dai, Guanghai Not yet recruiting No outcome recorded
Phase 2 NCT07779694 Oct 2026 → Dec 2028 expected rectal carcinoma Zhejiang University Not yet recruiting No outcome recorded
Phase 2 NCT07802418 Oct 2026 → Jun 2031 expected malignant pancreatic neoplasm Herlev Hospital Not yet recruiting No outcome recorded
Phase 2 NCT07802288 Sep 2026 → Apr 2029 expected gastroesophageal adenocarcinoma Tianjin Medical University Cancer Institute and Hospital Not yet recruiting No outcome recorded
Phase 2 NCT07815288 Sep 2026 → Dec 2029 expected colorectal adenocarcinoma Peking University Cancer Hospital & Institute Not yet recruiting No outcome recorded
Phase 2 NCT07828756 Sep 2026 → Oct 2027 expected malignant pancreatic neoplasm Tianjin Medical University Cancer Institute and Hospital Not yet recruiting No outcome recorded
Phase 2 NCT07847710 Sep 2026 → Mar 2028 expected intrahepatic cholangiocarcinoma The First Affiliated Hospital with Nanjing Medical University Recruiting No outcome recorded
Phase 2 NCT07800000 Sep 2026 → Sep 2028 expected anal canal squamous cell carcinoma Wang Xin Not yet recruiting No outcome recorded
Phase 2 NCT07833241 Sep 2026 → Sep 2028 expected pancreatic exocrine neoplasm Shanghai Zhongshan Hospital Not yet recruiting No outcome recorded
Show all 865 trials opens the full record — a long page
Phase 2/350 trials · 3 met primary · 6 missed
Phase 2/3 NCT07866313 Jun 2026 → Aug 2028 expected colorectal cancer Changhai Hospital Recruiting No outcome recorded
Phase 2/3 NCT07490262 Mar 2026 → Dec 2027 expected hepatocellular carcinoma Innovent Biopharmaceutical Technology (Hangzhou) Co., LTD. Recruiting No outcome recorded
Phase 2/3 NCT07392866 Mar 2026 → Mar 2030 expected hepatocellular carcinoma Nanjing Sanhome Pharmaceutical, Co., Ltd. Not yet recruiting No outcome recorded
Phase 2/3 NCT07251062 Dec 2025 → Dec 2029 expected esophageal squamous cell carcinoma CSPC Megalith Biopharmaceutical Co.,Ltd. Not yet recruiting No outcome recorded
Phase 2/3 NCT07309419 Dec 2025 → Jun 2030 expected hepatocellular carcinoma Shanghai Zhongshan Hospital Not yet recruiting No outcome recorded
Phase 2/3 NCT06841679 Aug 2025 → Sep 2030 expected gastroesophageal adenocarcinoma Beijing Biostar Pharmaceuticals Co., Ltd. Recruiting No outcome recorded
Phase 2/3 NCT06758830 Jan 2025 → Dec 2029 expected rectal cancer National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos Recruiting No outcome recorded
Phase 2/3 NCT06268327 Apr 2024 → Oct 2025 overdue breast cancer Assiut University Not yet recruiting No outcome recorded
Phase 2/3 NCT05976568 Sep 2023 → Sep 2027 expected hepatocellular carcinoma Qilu Pharmaceutical Co., Ltd. Not yet recruiting No outcome recorded
Phase 2/3 NCT05902533 Aug 2023 → Aug 2026 overdue anal carcinoma University of Cincinnati Active not recruiting No outcome recorded
Phase 3207 trials · 28 met primary · 24 missed
Phase 3 NCT07591493 Sep 2026 → Jun 2035 expected pancreatic neuroendocrine tumor Gustave Roussy, Cancer Campus, Grand Paris Not yet recruiting No outcome recorded
Phase 3 NCT07584135 May 2026 → Jan 2029 expected gastric adenocarcinoma NingBo Junyan Hongshi Biosciences Co., Ltd Recruiting No outcome recorded
Phase 3 NCT07590024 May 2026 → Dec 2030 expected nasopharyngeal carcinoma Cancer Institute and Hospital, Chinese Academy of Medical Sciences Recruiting No outcome recorded
Phase 3 NCT07340567 May 2026 → Nov 2032 expected colorectal cancer UNICANCER Not yet recruiting No outcome recorded
Phase 3 NCT06346197 Dec 2025 → May 2028 expected gastric cancer, metastatic malignant neoplasm Centre Leon Berard Recruiting No outcome recorded
Phase 3 NCT07238569 Dec 2025 → Dec 2029 expected nasopharyngeal carcinoma Sun Yat-sen University Not yet recruiting No outcome recorded
Phase 3 NCT07467330 Nov 2025 → Dec 2031 expected breast cancer Fujian Cancer Hospital Recruiting No outcome recorded
Phase 3 NCT07154069 Nov 2025 → Sep 2031 expected nasopharyngeal carcinoma Sun Yat-sen University Recruiting No outcome recorded
Phase 3 NCT07188025 Oct 2025 → Oct 2030 expected rectal cancer Erasmus Medical Center Recruiting No outcome recorded
Phase 3 NCT07248670 Oct 2025 → Dec 2031 expected nasopharyngeal carcinoma Chongqing University Cancer Hospital Active not recruiting No outcome recorded
Show all 207 trials opens the full record — a long page
Phase 428 trials
Phase 4 NCT07801027 Nov 2026 → Jan 2030 expected biliary tract cancer, gastric neoplasm, gastroesophageal junction adenocarcinoma, uterine cervix neoplasm Merck Sharp & Dohme LLC Not yet recruiting No outcome recorded
Phase 4 NCT07483060 Mar 2026 → Dec 2028 expected rectal cancer Vastra Gotaland Region Not yet recruiting No outcome recorded
Phase 4 NCT07158164 Aug 2025 → Jul 2027 expected breast neoplasm, colorectal neoplasm, head and neck neoplasm, intraepithelial neoplasia Rutgers, The State University of New Jersey Recruiting No outcome recorded
Phase 4 NCT06931808 Mar 2025 → Mar 2026 overdue rectum adenocarcinoma First Affiliated Hospital of Ningbo University Enrolling by invitation No outcome recorded
Phase 4 NCT06550453 Sep 2024 → Jan 2025 overdue colorectal carcinoma yangjianjun Recruiting No outcome recorded
Phase 4 NCT05203172 Jul 2022 → Jul 2029 expected cancer Pfizer Recruiting No outcome recorded
Phase 4 NCT04747951 Oct 2020 → Oct 2023 rectal cancer State Scientific Centre of Coloproctology, Russian Federation Unknown No outcome recorded
Phase 4 NCT04480268 Jul 2020 → Jan 2022 pancreatic ductal adenocarcinoma IRCCS San Raffaele Unknown No outcome recorded
Phase 4 NCT04767828 May 2020 → Jun 2022 thrombotic thrombocytopenic purpura Tianjin Medical University Cancer Institute and Hospital Unknown No outcome recorded
Phase 4 NCT04031885 Aug 2019 → Aug 2020 breast cancer Eli Lilly and Company Terminated No outcome recorded Stop: Enrollment
Phase not applicable53 trials · 1 missed
— NCT07854964 Oct 2026 → May 2030 expected — Tang-Du Hospital Not yet recruiting No outcome recorded
— NCT07859410 Oct 2026 → Oct 2028 expected gastroesophageal junction adenocarcinoma Anhui Medical University Not yet recruiting No outcome recorded
— NCT07563907 Jun 2026 → Dec 2030 expected rectal carcinoma Seoul National University Hospital Not yet recruiting No outcome recorded
— NCT07474103 Nov 2025 → Mar 2028 expected rectum adenocarcinoma Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Recruiting No outcome recorded
— NCT07334587 Sep 2025 → Feb 2026 overdue colorectal carcinoma Allama Iqbal Medical College Enrolling by invitation No outcome recorded
— NCT06434493 Nov 2024 → Jun 2028 expected cholangiocarcinoma The Christie NHS Foundation Trust Not yet recruiting No outcome recorded
— NCT06578052 Aug 2024 → Sep 2027 expected malignant pancreatic neoplasm Junjie Hang Recruiting No outcome recorded
— NCT06463548 Jul 2024 → Dec 2025 overdue biliary tract cancer Yunpeng Liu Not yet recruiting No outcome recorded
— NCT06052332 Feb 2024 → Dec 2029 expected — Jules Bordet Institute Recruiting No outcome recorded
— NCT06115733 Dec 2023 → Dec 2026 expected colorectal carcinoma Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine Not yet recruiting No outcome recorded
Phase not stated2 trials
— NCT00338247 Jul 2006 → Mar 2015 breast cancer Novartis Approved for marketing No outcome recorded
— NCT04220203 — HER2 positive breast carcinoma Pfizer Approved for marketing No outcome recorded
Comparator or background therapy852 trials
Phase 0 NCT07328087 Background Feb 2026 → Dec 2030 expected colorectal cancer Biogenea Pharmaceuticals Ltd. Recruiting No outcome recorded
Phase 0 NCT05108428 Background Dec 2021 → Oct 2023 overdue rectum adenocarcinoma H. Lee Moffitt Cancer Center and Research Institute Active not recruiting No outcome recorded
Phase 1 NCT07652242 Background Jul 2026 → Feb 2028 expected triple-negative breast carcinoma Immunomic Therapeutics, Inc. Recruiting No outcome recorded
Phase 1 NCT07024615 Background Oct 2025 → Jan 2028 expected pancreatic ductal adenocarcinoma Astellas Pharma Global Development, Inc. Recruiting No outcome recorded
Phase 1 NCT07114601 Background Aug 2025 → Apr 2030 expected breast neoplasm, colorectal neoplasm, endometrium neoplasm, gastric neoplasm +3 Eli Lilly and Company Recruiting No outcome recorded
Show all 852 trials opens the full record — a long page

Press releases naming this drug 23 releases

DateIssuerRelease
2023-12-19 Processa Pharmaceuticals Processa Pharmaceuticals Provides Interim Analysis from Ongoing Phase 1b Trial of Next Generation Capecitabine Showing Improved Safety Over Capecitabine processapharmaceuticals.com ↗
2023-12-13 Processa Pharmaceuticals Processa Pharmaceuticals Announces Successful Phase 2 Meeting with FDA for Next Generation Capecitabine processapharmaceuticals.com ↗
2023-11-06 Chugai Pharmaceutical Transfer and Future Marketing of Anti-Cancer Agent “Xeloda ® Tablets 300” in Japan chugai-pharm.co.jp ↗
2023-05-18 Processa Pharmaceuticals Processa Pharmaceuticals to Conduct Next Generation Chemotherapy-Capecitabine Phase 2 Trial Based on FDA Guidance and Project Optimus Oncology Initiative processapharmaceuticals.com ↗
2023-03-17 Processa Pharmaceuticals Processa Pharmaceuticals Announces First Patient Dosed in the 300 mg Dose Group with Next Generation Chemotherapy-Capecitabine processapharmaceuticals.com ↗
2022-11-01 Processa Pharmaceuticals Processa Successfully Identifies Next Generation Capecitabine Dosage Regimens for Phase 2B Trial processapharmaceuticals.com ↗
2022-04-20 Processa Pharmaceuticals Processa Pharmaceuticals Doses First Patient in Amended Phase 1B Protocol for PCS6422 Combined with Capecitabine (Next Generation Capecitabine) processapharmaceuticals.com ↗
2021-11-25 Ono Pharmaceutical Co., Ltd. ONO Receives Approval of Opdivo® (nivolumab) for Expanded Use for Two Indications in Japan - First-line Treatment of Unresectable Advanced or Recurrent Gastric Cancer in Combination with Chemotherapy - Adjuvant Treatment of Esophageal Cancer PDF(192 KB) @media screen and (max-width: 767px){ .mod__table-data { min-width: 100px !important; } } Ono Pharmaceutical Co., Ltd. (Osaka, Japan; President, Representative Director, Gyo Sagara; “ONO”) and Bristol-Myers Squibb K.K. (Shinjuku, Tokyo; President, Jean-Christophe Barland) today announced that ONO has received the approvals of Opdivo® (generic name: nivolumab) Intravenous Infusion (“Opdivo”), a human anti-PD-1 monoclonal antibody in Japan, for expanded use for the first-line treatment of unresectable advanced or recurrent gastric cancer in combination with chemotherapy, and adjuvant treatment of esophageal cancer, for a partial change in approved items of the manufacturing and marketing approval. 〈Approval for the first-line treatment of unresectable advanced or recurrent gastric cancer〉 This approval is based on the results from the following 2 clinical studies: CheckMate -649 study (ONO-4538-44): A global multi-center, randomized, open-label Phase 3 clinical study, evaluating Opdivo plus chemotherapy or Opdivo plus Yervoy (ipilimumab) combination compared to chemotherapy alone in patients with previously untreated, non-human epidermal growth factor receptor 2 (non-HER2)-positive, unresectable advanced or recurrent gastric cancer (GC), gastroesophageal junction cancer (GEJC) or esophageal adenocarcinoma (ESA), conducted on a world-wide basis including Japan, South Korea and Taiwan In this study, Opdivo plus chemotherapy showed a statistically significant and clinically meaningful improvement in overall survival (OS) both in all randomized patient population and OS in PD-L1 positive patients with a combined positive score (CPS) ≥5, one of the primary endpoints, versus chemotherapy. Furthermore, Opdivo plus chemotherapy demonstrated a statistically significant extension in progression-free survival (PFS) in PD-L1 positive patients with CPS ≥5, the other primary endpoint, versus chemotherapy. The safety profile of Opdivo plus chemotherapy in the study was consistent with the known safety profiles of the individual treatments. ATTRACTION-4 study (ONO-4538-37): A multi-center, randomized Phase 2/3 clinical study, evaluating Opdivo plus chemotherapy compared to placebo plus chemotherapy in patients with previously untreated, HER-2 negative, unresectable advanced or recurrent GC or GEJC, conducted in Japan, South Korea and Taiwan In this study, Opdivo plus chemotherapy showed a statistically significant extension in PFS, one of the primary endpoints, versus placebo plus chemotherapy. On the other hand, Opdivo plus chemotherapy did not demonstrate a statistically significance in OS, the other of the primary endpoints. The safety profile of Opdivo plus chemotherapy in the study was consistent with the known safety profiles of the individual treatments. About CheckMate -649 study (ONO-4538-44) Checkmate -649 is a multi-center, randomized, open-label Phase 3 clinical study, evaluating Opdivo plus chemotherapy or Opdivo plus Yervoy combination compared to chemotherapy alone in patients with previously untreated, non-HER2-positive, unresectable advanced or recurrent gastric cancer, gastroesophageal junction cancer or esophageal adenocarcinoma. Patients in the Opdivo plus chemotherapy arm received Opdivo 240 mg plus fluorouracil, calcium folinate and oxaliplatin (FOLFOX) every two weeks or Opdivo 360 mg plus capecitabine and oxaliplatin (CapeOX) every three weeks. Patients in the chemotherapy arm received FOLFOX or CapeOX every two or three weeks, respectively. All patients continued treatment up to two years or until disease progression, unacceptable toxicity or withdrawal of consent. The primary endpoints of the study are overall survival (OS) in PD-L1 positive patients with a combined positive score (CPS) ≥ 5 treated with Opdivo plus chemotherapy and progression-free survival (PFS) in CPS ≥ 5 patients treated with Opdivo plus chemotherapy. Key secondary endpoint is OS in CPS ≥ 1 and all-randomized patients treated with Opdivo plus chemotherapy. About ATTRACTION-4 study (ONO-4538-37) ATTRACTION-4 study is a multi-center, randomized Phase 2/3 clinical study, evaluating Opdivo plus chemotherapy (oxaliplatin + S-1 or capecitabine) compared to placebo plus chemotherapy in patients with previously untreated, HER2 negative unresectable advanced or recurrent gastric cancer or gastroesophageal junction cancer. Patients received Opdivo 360 mg or placebo every 3 weeks until disease progression or unacceptable toxicity is observed. The primary endpoints of the study are progression-free survival (PFS) and overall survival (OS). About Gastric cancer It is estimated that about 138,000 new cases 1) are diagnosed with gastric cancer per year in Japan (about 1,089,000 cases worldwide 2) ) and approximately 46,000 deaths 1) (about 768,000 worldwide 2) ) per year resulting from this disease 1) , which is the 2nd most common type of cancer after lung cancer in Japan. As there has been little progression in the standard of care of first-line chemotherapy for the HER2 negative unresectable, advanced or recurrent gastric cancer in the past decade in Japan, an innovative treatment option is needed in this patient population. Globocan 2020: Stomach Cancer, Japan, World Health Organization https://gco.iarc.fr/today/data/factsheets/populations/392-japan-fact-sheets.pdf Globocan 2020: Stomach Cancer, World, World Health Organization https://gco.iarc.fr/today/data/factsheets/populations/900-world-fact-sheets.pdf 〈Approval for the adjuvant treatment of esophageal cancer〉 This approval is based on the results from a global multi-center, randomized, double-blind Phase 3 clinical study, CheckMate -577 study (ONO-4538-43), evaluating Opdivo monotherapy as an adjuvant treatment in patients with resected esophageal cancer (ESC) or gastroesophageal junction cancer (GEJC) compared to placebo. In this study, Opdivo showed a statistically significant improvement in disease-free survival (DFS), the primary endpoint of the study, compared to placebo. The safety profile of Opdivo in this study was consistent with previously reported studies of Opdivo monotherapy. About CheckMate -577 study (ONO-4538-43) CheckMate -577 study is a global multi-center, randomized, double-blind Phase 3 clinical study, evaluating Opdivo monotherapy as an adjuvant treatment in patients with resected esophageal cancer or gastroesophageal junction cancer (GEJC) who have received chemoradiation therapy (CRT) and have not achieved a pathological complete response. Following neoadjuvant CRT and complete tumor surgical resection (also known as trimodality therapy), patients were randomized to receive Opdivo or placebo. In patients receiving Opdivo, it was administered at 240 mg every two weeks for 16 weeks followed by Opdivo 480 mg every four weeks until disease recurrence, unacceptable toxicity or withdrawal of consent, with a maximum of one year total treatment duration. The primary endpoint of the study is disease-free survival (DFS) and the secondary endpoint is overall survival (OS). About esophageal cancer Esophageal cancer is a malignant tumor that occurs in the inner layer (mucosa) of the esophagus and grows outside (toward the deeper layer). There are two main histological types of esophageal cancer; squamous cell carcinoma (SCC) and adenocarcinoma. SCC is the predominant type accounting for about 90% of all esophageal cancer in Japan. It is estimated that about 26,000 new cases1) are diagnosed with esophageal cancer per year in Japan (about 604,000 cases worldwide 2) ) and approximately 12,000 deaths 1) (about 544,000 worldwide 2) ) per year resulting from this disease. In Japan, radical resection following neoadjuvant therapy is performed as a treatment for resectable locally advanced esophageal cancer that does not have distant metastasis, but recurrence has been observed in 28-47% after radical resection. Furthermore, since the prognosis of recurrent cases after radical resection of esophageal cancer is extremely poor 3) , it is considered that there is a high medical need for postoperative adjuvant therapy aimed at suppressing recurrence. Globocan 2020: Esophageal Cancer, Japan, World Health Organization Available at: https://gco.iarc.fr/today/data/factsheets/populations/392-japan-fact-sheets.pdf Globocan 2020: Esophageal Cancer, World, World Health Organization Available at: https://gco.iarc.fr/today/data/factsheets/populations/900-world-fact-sheets.pdf Guideline for Diagnosis and Treatment of Carcinoma of the Esophagus 2017, The Japan Esophageal Society Overview of Opdivo® Intravenous Infusion Product name Opdivo® Intravenous Infusion 20mg, 100mg, 120mg and 240mg Generic name (JAN) Nivolumab (Genetical recombination) Indication Melanoma Unresectable, advanced or recurrent non-small cell lung cancer Unresectable or metastatic renal cell carcinoma Recurrent or refractory classical Hodgkin lymphoma Recurrent or metastatic head and neck cancer Unresectable advanced or recurrent gastric cancer that has progressed after chemotherapy Unresectable advanced or recurrent malignant pleural mesothelioma Microsatellite instability high (MSI-High) unresectable advanced or recurrent colorectal cancer that has progressed after chemotherapy Unresectable advanced or recurrent esophageal cancer that has progressed after chemotherapy Adjuvant treatment of esophageal cancer Dosage and administration 〈Melanoma〉 Usually, for adults, administer at 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. In the adjuvant treatment of melanoma, the administration period does not exceed 12 months. In combination therapy with ipilimumab for unresectable melanoma, usually, for adults, administer 80 mg of nivolumab every 3 weeks for 4 doses. After that, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. 〈Unresectable, advanced or recurrent non-small cell lung cancer , and unresectable advanced or recurrent gastric cancer that has progressed after chemotherapy 〉 Usually, for adults, administer at 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. In combination therapy with other anti-tumor drugs, usually, for adults, administer 240 mg of nivolumab every 2 weeks or 360 mg every 3 weeks as intravenous infusion. 〈Unresectable or metastatic renal cell carcinoma〉 Usually, for adults, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. In combination with cabozantinib, usually, for adults, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. In combination therapy with ipilimumab for unresectable or metastatic renal cell carcinoma previously untreated with chemotherapy, usually, for adults, administer 240 mg of nivolumab as intravenous infusion every 3 weeks for 4 doses. After that, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. 〈Recurrent or refractory classical Hodgkin lymphoma〉 Usually, for adults, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. Usually for pediatrics, administer 3 mg/kg (body weight) of nivolumab every 2 weeks as intravenous infusion. For pediatrics weighing 40 kg (body weight) or more, nivolumab can be administered at 240 mg of every 2 weeks or 480 mg every 4 weeks as intravenous infusion. 〈Recurrent or metastatic head and neck cancer〉 Usually, for adults, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. 〈Unresectable advanced or recurrent malignant pleural mesothelioma〉 Usually, for adults, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. In combination therapy with ipilimumab, usually, for adults, administer 240 mg of nivolumab every 2 weeks or 360 mg every 3 weeks as intravenous infusion. 〈Microsatellite instability high (MSI-High) unresectable advanced or recurrent colorectal cancer that has progressed after chemotherapy〉 Usually, for adults, administer at 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. In combination therapy with ipilimumab, usually, for adults, administer 240 mg of nivolumab as intravenous infusion every 3 weeks for 4 doses. After that, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. 〈Unresectable advanced or recurrent esophageal cancer that has progressed after chemotherapy, and adjuvant treatment of esophageal cancer〉 Usually, for adults, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. In the adjuvant treatment of esophageal cancer, the administration period does not exceed 12 months. 〈 Recurrent or metastatic head and neck cancer, unresectable advanced or recurrent gastric cancer that has progressed after chemotherapy, and unresectable advanced or recurrent esophageal cancer that has progressed after chemotherapy〉 Usually, for adults, administer 240 mg of nivolumab every 2 weeks or 480 mg every 4 weeks as intravenous infusion. Manufacturer/distributor Ono Pharmaceutical Co., Ltd. Co-promotion Bristol-Myers Squibb K.K. Note: Underlined parts show the revised ones according to this approval. About Opdivo Opdivo is a programmed death-1 (PD-1) immune checkpoint inhibitor that is designed to uniquely harness the body’s own immune system to help restore anti-tumor immune response by blocking the interaction between PD-1 and its ligands. By harnessing the body’s own immune system to fight cancer, Opdivo has become an important treatment option across multiple cancers since the approval for the treatment of melanoma in Japan in July 2014. Opdivo is currently approved in more than 65 countries, including Japan, South Korea, Taiwan, China, the US and European Union. In Japan, ONO launched Opdivo for the treatment of unresectable melanoma in September 2014. Thereafter, Opdivo received an approval for additional indications of unresectable, advanced or recurrent non-small cell lung cancer in December 2015, unresectable or metastatic renal cell carcinoma in August 2016, relapsed or refractory classical Hodgkin lymphoma in December 2016, recurrent or metastatic head and neck cancer in March 2017, unresectable advanced or recurrent gastric cancer which has progressed after chemotherapy in September 2017, unresectable advanced or recurrent malignant pleural mesothelioma which has progressed after chemotherapy in August 2018, and microsatellite instability high (MSI-High) unresectable advanced or recurrent colorectal cancer that has progressed following chemotherapy and unresectable advanced or recurrent esophageal cancer that has progressed following chemotherapy in February 2020. In addition, ONO has submitted supplemental applications for the adjuvant treatment of urothelial cancer and cancer of unknown primary, and is conducting clinical development program including hepatocellular carcinoma, ovarian cancer, bladder cancer, prostate cancer, pancreatic cancer, biliary tract cancer, etc. About the ONO and Bristol-Myers Squibb Collaboration In 2011, through a collaboration agreement with Bristol-Myers Squibb (BMS), ONO granted BMS its territorial rights to develop and commercialize Opdivo globally except in Japan, South Korea and Taiwan, where ONO had retained all rights to Opdivo except the US at the time. In July 2014, ONO and BMS further expanded the companies’ strategic collaboration agreement to jointly develop and commercialize multiple immunotherapies – as single agent and combination regimens – for patients with cancer in Japan, South Korea and Taiwan. Back to List ono-pharma.com ↗
2021-11-04 Processa Pharmaceuticals Processa Pharmaceuticals Announces Next Generation Capecitabine (Combination of PCS6422 and Capecitabine) Inhibits DPD in Phase 1b Interim Analysis processapharmaceuticals.com ↗
2019-04-08 Ascelia Pharma AB Encouraging results from the Phase I combination study with Oncoral and oral capecitabine published in the journal Cancer Chemotherapy and Pharmacology ascelia.com ↗
2018-10-18 Chugai Pharmaceutical Xeloda ® Adherence Support App Contributes to Improving Communication between Cancer Patients and Healthcare Providers chugai-pharm.co.jp ↗
2018-04-02 Puma Biotechnology, Inc. NCCN Guidelines for Central Nervous System Cancers Include NERLYNX® (neratinib) in Combination with Capecitabine or Paclitaxel as Treatment Options for Patients with Breast Cancer Brain Metastases pumabiotechnology.com ↗

Evidence & citations 34 cited values

Every value below carries the sentence it was read from. 2,383 sources stand behind the page.

FieldValueCited text
Known as Capecitabine “RCT Cap 50 will combine radiotherapy at a dose of 50 Gy by either conventional 3D or Intensity-Modulated RadioTherapy (IMRT) (2 Gy per fraction, 5 fractions per week during 5...” NCT04749108 ↗
2345

“Patients (pts) with HER2-positive (gene amplification or increased copy numbers based on predefined criteria) advanced GC were randomly allocated 1:1 to receive LAP 1250mg per...” PMID 25694417 ↗ Feb 2015

“RCT Cap 50 will combine radiotherapy at a dose of 50 Gy by either conventional 3D or IMRT (2 Gy per fraction, 5 fractions per week during 5 weeks / 44 Gy in mini pelvis, and...” NCT01333709 ↗

“After achieving an objective response (ORR) with the combination of MRG003 and Tislelizumab, maintenance therapy will consist of Capecitabine (650 mg/m², administered twice...” NCT07331428 ↗

“The dosing regimen during the dose escalation phase will include three different doses of fruquintinib (3 mg, 4 mg and 5 mg, per oral, once per day days 1-14) + sintilimab,...” PMID 41005780 ↗ Sep 2025

“After achieving objective tumor response or stable disease after 3 cycles of capecitabine and oxaliplatin or 4 cycles of 5-fluorouracil and oxaliplatin with or without...” PMID 41837962 ↗ Apr 2026

“Any of the following single-agent chemotherapy may be given at the discretion of the investigator, with a cycle length not to exceed four weeks: Capecitabine, Vinorelbine,...” NCT01156753 ↗

“Participants will receive 6 cycles of a standard intravenous or oral chemotherapy regimen or an Antibody-Drug Conjugate (ADC), selected by the investigator from...” NCT07371910 ↗

“The neoadjuvant treatment regimen will consist of Oxaliplatin at a dose of 130mg/m2, administered intravenously over a period of more than 2 hours on Day 1, every 3 weeks; and...” NCT06014372 ↗

“The main objective of the SIRTCI study is to evaluate the safety and efficacy of the combination chemotherapy (XELOX: Capecitabine plus oxaliplatin), anti-angiogenic...” NCT04659382 ↗

“CRT (1 cycle CT: Xelox or SOX, Q21d×1, Followed by RT: 45 Gray (Gy), 5d/week×5 with capecitabine or S1, Followed by 3 cycles CT: Xelox or SOX, Q21d×3) will be applied to...” NCT03680261 ↗

Show 2,335 more sources

Known as 5-FU “5-FU (Capecitabine) Consolidation chemotherapy 3 cycles” NCT07563907 ↗
Known as CAP “Patients (pts) with HER2-positive (gene amplification or increased copy numbers based on predefined criteria) advanced GC were randomly allocated 1:1 to receive LAP 1250mg per...” PMID 25694417 ↗ Feb 2015
10

“To evaluate the clinical efficacy of adding temozolomide (TMZ) to preoperative capecitabine (CAP)-based chemoradiotherapy in patients with locally advanced rectal cancer (LARC)...” PMID 36376167 ↗ Nov 2022

“AIM OF THE STUDY: Evaluation of the impact of a de-escaleted chemotherapy regimen consisting of capecitabine (Cap) on invasive disease-free survival (iDFS) in patients ≥65...” PMID 37797387 ↗ Sep 2023

“PURPOSE: We performed a UGT1A1 genotype-guided study to determine the maximum tolerated dose (MTD) and evaluate the toxicities and pharmacokinetics of the combination of...” PMID 24114122 ↗ Oct 2013

“A Pivotal Phase II Clinical Trial of Utidelone Injection (UTD1) Plus Capecitabine (CAP) in HER2-negative Breast Cancer Patients With Brain Metastases” NCT06764940 ↗

“This is an open label study to assess the efficacy of capecitabine (CAP) and temozolomide (TMZ) in recurrent pituitary adenomas.” NCT03930771 ↗

“capecitabine (CAP) in patients with previously treated unresectable, locally advanced or metastatic breast cancer.” PMID 28220020 ↗ Feb 2017

“bevacizumab (BEV) to preoperative capecitabine (CAP)-based CRT in LARC” PMID 25886378 ↗ Feb 2015

“All pts were treated with Capecitabine (Cap) 625-825 mg/m2/12h M-F.” NCT01366118 ↗

“gemcitabine (Gem) plus capecitabine (Cap) versus single-agent Gem” PMID 18669454 ↗ Aug 2008

“capecitabine (CAP)” PMID 37402471 ↗ Jul 2023

Known as CAPE “Patients receive docetaxel as in Arm 1A and oral capecitabine (cape) twice daily on days 1-14 every 3 weeks for up to 4 cycles.” NCT00408408 ↗
3

“We investigate the replacement of 5-FU by the oral pro-drug capecitabine (cape) within a randomized phase III trial.” NCT01500993 ↗

“De-escalation treatment (capecitabine [CAPE] for 6 months).” NCT07340567 ↗

“Capecitabine (CAPE) or Xeloda® (XEL) + oxaliplatin (OX)” NCT00551213 ↗

Known as Capecitabina ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Capecitabine (Cap) “Capecitabine (Cap)” NCT03262935 ↗
Known as Capecitabine (XELODA ,Roche) “Capecitabine (XELODA ,Roche)” NCT02027363 ↗
Known as Capecitabine (Xeloda○R), company: Roche “Capecitabine (Xeloda○R), company: Roche” NCT01558011 ↗
Known as Capecitabine accord ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Capecitabine component of xeliri capecitibine ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Capecitabine component of xelox ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Capecitabine medac ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Capecitabine sun ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Capecitabine tablets “Drug: Capecitabine tablets” NCT05901935 ↗
1

“Drug: Capecitabine Tablets” NCT07606599 ↗

Known as Capecitabine teva ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Capecitabine(Xeloda) “capecitabine (Xeloda®)” NCT01067053 ↗
8

“Capecitabine(Xeloda®)” NCT00853684 ↗

“Capecitabine (Xeloda)” NCT01195298 ↗

“Capecitabine (Xeloda)” NCT01640665 ↗

“Capecitabine (Xeloda)” NCT01196455 ↗

“Capecitabine (Xeloda)” NCT01941771 ↗

“Capecitabine: Xeloda” NCT01642771 ↗

“Capecitabine, Xeloda” NCT00961571 ↗

“Capecitabine: Xeloda” NCT01802970 ↗

Known as Capecitibine ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Capecytabine ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Capiibine ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Captabin ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Ecansya ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as Ecansya (previously capecitabine krka) ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as metroCap “RIBBON-LA-01 is a single-arm, open-label, phase 2 clinical trial of maintenance tislelizumab and metronomic capecitabine (metroCap) for 52 weeks after IC and CCRT” NCT06093061 ↗
Known as NSC-759853 ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗
Known as RO 09-1978/000 ChEMBL registry synonym — accepted as the source's own label CHEMBL1773 ↗