Catequentinib
Small molecule targets CYP3A4, FGFR1, FLT4, KDR, KIT, MET, PDGFRA, PDGFRB via inhibition
Trials 472 · started per year
News releases announcing trial results or a regulatory action · 27
| Date | Issuer | Release |
|---|---|---|
| 2025-12-26 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Regulatory 安罗替尼联合派安普利单抗获批肝癌一线治疗,“免疫+抗血管”协同增效为患者带来新希望 cttq.com ↗
12月25日,正大天晴1类创新药盐酸安罗替尼胶囊(福可维®)的第十个适应症——联合派安普利单抗注射液(安尼可®)一线治疗晚期肝细胞癌,收到国家药品监督管理局颁发的药品注册批件,这也是派安普利单抗获批上市的第五个适应症。 |
| 2025-09-10 | Hansoh BioMedical R&D Company | Results 2025 WCLC | 翰森制药阿美乐®18项创新研究亮相国际学术大会 hansoh.cn ↗
数据截止时, 14例可评估疗效,中位随访时间为23个月(95%CI:8. 0-31. 0),mPFS为25个月(95%CI:11. 0 -NR). |
| 2025-07-09 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 《柳叶刀》子刊:儿童肉瘤精准治疗迈出关键一步,安罗替尼再添循证 cttq.com ↗
近日,正大天晴1类新药——盐酸安罗替尼胶囊用于治疗高危、复发或难治性儿童肉瘤患者的临床试验结果,发表于《柳叶刀》旗下刊物《电子临床医学》(eClinical Medicine)[1]。 |
| 2025-07-03 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results Molecular Cancer(IF33.5):得福组合去化疗方案为食管鳞癌患者提供治疗新思路 cttq.com ↗
研究结果显示,经确认客观缓解率(ORR)为56.5%,疾病控制率(DCR)达到91.3%,中位无进展生存期(PFS)达到15.74个月,中位总生存期(OS)为20.57个月,展现了良好的生存获益。 |
| 2025-06-11 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Regulatory 突破“癌王”治疗困境!正大天晴TQB2868联合方案获批Ⅲ期临床,剑指胰腺癌一线免疫治疗空白 cttq.com ↗
6月11日,正大天晴宣布自主研发的1类创新药TQB2868注射液联合盐酸安罗替尼胶囊及化疗,用于转移性胰腺导管腺癌(mPDAC)一线治疗方案,已获得国家药品监督管理局药品审评中心(CDE)批准开展Ⅲ期注册临床试验。 |
| 2025-06-05 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 去化疗新选择!“得福组合”一线治疗三阴性乳腺癌展现临床获益趋势 cttq.com ↗
中位总生存期(OS):联合组35.81个月vs.对照组21.03个月(HR=0.78;95%CI:0.49-1.24;P=0.2625),较对照组提升近15个月; |
| 2025-06-03 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results ASCO LBA重磅发布:全球首个靶免巩固治疗Ⅲ期非小细胞肺癌研究,中位PFS突破15个月刷新记录 cttq.com ↗
试验组1:中位PFS 为15.1个月,对照组4.2个月(HR=0.49, 95%CI 0.36-0.66, P<0.001),疾病进展或死亡风险降低51%。 |
| 2025-06-02 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results ASCO 重磅! “得福组合”头对头战胜K药,一线治疗PD-L1阳性非小细胞肺癌取得重大突破 cttq.com ↗
在全人群中,“得福组合”中位PFS达到11.0个月,较帕博利珠单抗治疗提升3.9个月,疾病进展或死亡风险降低30%(HR=0.70)。 |
| 2025-05-31 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results ASCO LBA: 脑胶质瘤协同增效新策略 安罗替尼联合方案突破性研究成果首次公开 cttq.com ↗
安罗替尼组独立数据委员会(IRC)评估的中位无进展生存期(mPFS)达9.89个月(95% CI 9.10-11.56),较安慰剂组(5.85个月)显著提升,疾病进展或死亡风险降低41%(HR=0.59,p=0.0018)。 |
| 2025-05-28 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 破解胰腺癌免疫逃逸!正大天晴PD-1/TGF-β双功能融合蛋白联合疗法Ⅱ期数据亮相ASCO cttq.com ↗
安全耐受性良好,3级及以上不良反应发生率为52.5%(AG化疗方案为68.1%-77%)。 |
| 2025-05-26 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 从“跟随创新”到“引领突破” 安罗替尼联合化疗一线治疗软组织肉瘤mPFS延长5.5个月 cttq.com ↗
初步结果显示,试验组较对照组显著延长中位无进展生存期(mPFS)(8.57个月vs 3.02个月;HR=0.30, 95%CI 0.21-0.44, P<0.001),客观缓解率(ORR)提升近6倍(17.8% vs 2.9%),疾病控制率(DCR)显著提高(79.3% vs 54.7%)。 |
| 2025-05-24 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results “国药之光”领衔12大ORAL刷屏ASCO,中国生物制药引领中国创新药企冲刺全球新 cttq.com ↗
研究结果显示,安罗替尼联合治疗组患者中位PFS延长约5.5个月,客观缓解率(ORR)、疾病控制率(DCR)显著提高,总生存期(OS)已显示出获益趋势。 |
| 2025-05-23 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 首个战胜PD-1联合化疗研究数据公开!正大天晴 “得福组合”一线治疗肺鳞癌获显著阳性结果 cttq.com ↗ |
| 2025-05-13 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 柳叶刀肿瘤:安罗替尼联合派安普利单抗一线治疗肝细胞癌双终点阳性 cttq.com ↗
研究显示,该治疗方案较对照组疾病进展风险降低48%,死亡风险降低31%,主要终点无进展生存期(PFS)和总生存期(OS)均取得阳性结果[1]。 |
| 2025-04-01 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 2025 ELCC | 安罗替尼联合治疗如何“精准制导”EGFR突变晚期非小细胞肺癌? cttq.com ↗
12例患者完成首次疗效评估,ORR为33.3%,DCR达100%。 |
| 2025-01-20 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 全球首个!中国团队发现EGFR突变型肺癌耐药新机制,研究见刊《J HEMATOL ONCOL》 cttq.com ↗
研究结果显示,患者的中位无进展生存期(mPFS)为9.1个月,6个月和12个月的PFS率分别为68.5%和38.8%。 |
| 2024-12-23 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Regulatory 2024新药成绩单,正大天晴领跑肿瘤1类创新药赛道 cttq.com ↗
11月,贝莫苏拜单抗联合安罗替胶囊获批新适应症。 |
| 2024-12-16 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 2024 SABCS|正大天晴公布安罗替尼治疗乳腺癌最新数据 cttq.com ↗
40例疗效可评估患者的主要终点客观缓解率(ORR)为75.0%,次要终点疾病控制率(DCR)为97.5%,中位无进展生存期(PFS)为10.64个月,中位总生存期(OS)尚未达到。 |
| 2024-12-09 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 2024 ESMO ASIA|正大天晴安罗替尼一线治疗消化道肿瘤数据披露 cttq.com ↗
客观缓解率(ORR)、疾病控制率(DCR)分别为48.3%和89.7%,中位无进展生存期(PFS)、中位总生存期(OS)分别为8.6个月和23.2个月。 |
| 2024-11-22 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Regulatory 一线治疗晚期肝细胞癌申报上市,安罗替尼正式进入消化道肿瘤领域 cttq.com ↗
11月21日,正大天晴自主研发1类创新药盐酸安罗替尼胶囊联合派安普利单抗注射液一线治疗晚期肝细胞癌的上市申请获得国家药品监督管理局药品审评中心(CDE)受理,代表安罗替尼正式进入消化道肿瘤领域。 |
| 2024-10-10 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 聚焦放疗前沿,正大天晴2款创新药最新数据亮相2024 ASTRO cttq.com ↗
试验组的中位无进展生存期(PFS)为10.05个月,1年总生存率为75.45%,2年总生存率为39.41%。 |
| 2024-09-18 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 双终点阳性!正大天晴安罗替尼联合派安普利单抗一线治疗晚期肝癌重要突破闪耀2024ESMO cttq.com ↗
研究结果显示,试验组中位无进展生存期(PFS)为6.9个月,对照组为2.8个月,疾病进展风险显著降低了47%。 |
| 2024-08-29 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 盐酸安罗替尼胶囊联合派安普利单抗用于晚期肝细胞癌一线治疗III期研究取得阳性结果 cttq.com ↗
本研究的期中分析结果显示,相较于索拉非尼,盐酸安罗替尼胶囊联合派安普利单抗一线治疗晚期肝细胞癌可显著降低患者的疾病进展或死亡风险,显著延长患者无进展生存期、总生存期。 |
| 2024-05-11 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Regulatory 天晴速度!1类新药贝莫苏拜单抗首批发货 cttq.com ↗
此外,公司近期已向国家药品监督管理局药品审评中心(CDE)提交了盐酸安罗替尼胶囊和贝莫苏拜单抗注射液新适应症的上市申请,并获得受理,用于既往接受过一、二线化疗方案治疗失败或不能耐受的非微卫星高度不稳定(非MSI-H)或非DNA错配修复缺陷(非dMMR)的复发性或转移性子宫内膜癌。 |
| 2024-03-20 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Results 新里程!正大天晴1类新药安罗替尼治疗妇科肿瘤伴肝转移研究成果解读 cttq.com ↗
结果显示,安罗替尼治疗妇科肿瘤伴肝转移的中位PFS达5.27个月, 卵巢癌和宫颈癌分别为6.3个月和6.7个月。 |
| 2022-08-04 | Hansoh BioMedical R&D Company | Results 2022 WCLC | 翰森制药阿美替尼21篇摘要闪耀登顶 原研之光展现中国创新力量 hansoh.cn ↗
11例患者均达到PR,总体ORR为100%(11/11);7例脑转移患者接受颅内靶病灶评估,其中5例达到PR,2名SD,iORR为71. 4%(5/7),iDCR为100%(7/7). |
| 2022-07-01 | Lyvgen Biopharma Holdings Limited | Regulatory Dr. C. Hubert Chan, Chief Medical Officer of Lyvgen Biopharma: Innovation in Clinical Development for the Breakthrough Cancer Immunotherapy of Next-Generation IO Agonistic Antibodies lyvgen.com ↗
In addition, the combination of LVGN6051 and Anlotinib (VEGFR-TKI) for the treatment of sarcoma has been approved in China and the first-in-patient dosing is expected soon. |
All press releases naming this drug 27 releases
| Date | Issuer | Release |
|---|---|---|
| 2025-12-26 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 安罗替尼联合派安普利单抗获批肝癌一线治疗,“免疫+抗血管”协同增效为患者带来新希望 cttq.com ↗ |
| 2025-09-10 | Hansoh BioMedical R&D Company | 2025 WCLC | 翰森制药阿美乐®18项创新研究亮相国际学术大会 hansoh.cn ↗ |
| 2025-07-09 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 《柳叶刀》子刊:儿童肉瘤精准治疗迈出关键一步,安罗替尼再添循证 cttq.com ↗ |
| 2025-07-03 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Molecular Cancer(IF33.5):得福组合去化疗方案为食管鳞癌患者提供治疗新思路 cttq.com ↗ |
| 2025-06-11 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 突破“癌王”治疗困境!正大天晴TQB2868联合方案获批Ⅲ期临床,剑指胰腺癌一线免疫治疗空白 cttq.com ↗ |
| 2025-06-05 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 去化疗新选择!“得福组合”一线治疗三阴性乳腺癌展现临床获益趋势 cttq.com ↗ |
| 2025-06-03 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | ASCO LBA重磅发布:全球首个靶免巩固治疗Ⅲ期非小细胞肺癌研究,中位PFS突破15个月刷新记录 cttq.com ↗ |
| 2025-06-02 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | ASCO 重磅! “得福组合”头对头战胜K药,一线治疗PD-L1阳性非小细胞肺癌取得重大突破 cttq.com ↗ |
| 2025-05-31 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | ASCO LBA: 脑胶质瘤协同增效新策略 安罗替尼联合方案突破性研究成果首次公开 cttq.com ↗ |
| 2025-05-28 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 破解胰腺癌免疫逃逸!正大天晴PD-1/TGF-β双功能融合蛋白联合疗法Ⅱ期数据亮相ASCO cttq.com ↗ |
| 2025-05-26 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 从“跟随创新”到“引领突破” 安罗替尼联合化疗一线治疗软组织肉瘤mPFS延长5.5个月 cttq.com ↗ |
| 2025-05-24 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | “国药之光”领衔12大ORAL刷屏ASCO,中国生物制药引领中国创新药企冲刺全球新 cttq.com ↗ |
| 2025-05-23 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 首个战胜PD-1联合化疗研究数据公开!正大天晴 “得福组合”一线治疗肺鳞癌获显著阳性结果 cttq.com ↗ |
| 2025-05-13 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 柳叶刀肿瘤:安罗替尼联合派安普利单抗一线治疗肝细胞癌双终点阳性 cttq.com ↗ |
| 2025-04-01 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 2025 ELCC | 安罗替尼联合治疗如何“精准制导”EGFR突变晚期非小细胞肺癌? cttq.com ↗ |
| 2025-01-20 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 全球首个!中国团队发现EGFR突变型肺癌耐药新机制,研究见刊《J HEMATOL ONCOL》 cttq.com ↗ |
| 2024-12-23 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 2024新药成绩单,正大天晴领跑肿瘤1类创新药赛道 cttq.com ↗ |
| 2024-12-16 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 2024 SABCS|正大天晴公布安罗替尼治疗乳腺癌最新数据 cttq.com ↗ |
| 2024-12-09 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 2024 ESMO ASIA|正大天晴安罗替尼一线治疗消化道肿瘤数据披露 cttq.com ↗ |
| 2024-11-22 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 一线治疗晚期肝细胞癌申报上市,安罗替尼正式进入消化道肿瘤领域 cttq.com ↗ |
| 2024-10-10 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 聚焦放疗前沿,正大天晴2款创新药最新数据亮相2024 ASTRO cttq.com ↗ |
| 2024-09-18 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 双终点阳性!正大天晴安罗替尼联合派安普利单抗一线治疗晚期肝癌重要突破闪耀2024ESMO cttq.com ↗ |
| 2024-08-29 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 盐酸安罗替尼胶囊联合派安普利单抗用于晚期肝细胞癌一线治疗III期研究取得阳性结果 cttq.com ↗ |
| 2024-05-11 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 天晴速度!1类新药贝莫苏拜单抗首批发货 cttq.com ↗ |
| 2024-03-20 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | 新里程!正大天晴1类新药安罗替尼治疗妇科肿瘤伴肝转移研究成果解读 cttq.com ↗ |
| 2022-08-04 | Hansoh BioMedical R&D Company | 2022 WCLC | 翰森制药阿美替尼21篇摘要闪耀登顶 原研之光展现中国创新力量 hansoh.cn ↗ |
| 2022-07-01 | Lyvgen Biopharma Holdings Limited | Dr. C. Hubert Chan, Chief Medical Officer of Lyvgen Biopharma: Innovation in Clinical Development for the Breakthrough Cancer Immunotherapy of Next-Generation IO Agonistic Antibodies lyvgen.com ↗ |
Evidence & citations 23 cited values
Every value below carries the sentence it was read from. 490 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | Catequentinib | “A Phase III Study of AL3818 (Anlotinib, Catequentinib) Hydrochloride Monotherapy in Subjects With Metastatic or Advanced Alveolar Soft Part Sarcoma, Leiomyosarcoma and Synovial Sarcoma” NCT03016819 ↗2“A Phase 1/2a Evaluation of the Safety and Efficacy of Adding AL3818 (Catequentinib) to Nivolumab in Solid Tumors” NCT04165330 ↗ “Catequentinib Hydrochloride (AL3818) Drug-Drug Interaction Study in Healthy Volunteers” NCT07438886 ↗ |
| Known as | AL-3818 DIHYDROCHLORIDE | ChEMBL registry synonym — accepted as the source's own label CHEMBL4303201 ↗ |
| Known as | AL3818 | “The purpose of this study is to assess the safety and efficacy of Anlotinib (AL3818) combined with pembrolizumab (MK-3475) in treatment-naïve adults with no prior systemic...” NCT04164745 ↗13“Anlotinib (AL3818) is a kind of innovative medicines approved by State Food and Drug Administration(SFDA:2011L00661) which was researched by Jiangsu Chia-tai Tianqing...” NCT03768037 ↗ “Anlotinib (AL3818) is an inhibitor targeting multiple receptor tyrosine kinases involved in tumour progression, especially VEGFR 2/3, PDGFRα/β and c-Kit.” NCT04438902 ↗ “Allotinib (AL3818) is manufactured by Zhengda Tianqing Pharmaceutical Group Co., LTD. (CTTQ; Lianyungang, Jiangsu, China) self-developed TKI drugs” NCT06429397 ↗ “BACKGROUND: Anlotinib (AL3818) is a novel multitarget tyrosine kinase inhibitor, inhibiting tumour angiogenesis and proliferative signalling.” PMID 29438373 ↗ Feb 2018 “A Phase II Study of Anlotinib(AL3818) in Patients With Advanced Renal Cell Carcinoma(RCC) That Have Failed Or Are Intolerant To TKIs Therapy” NCT02072044 ↗ “Catequentinib Hydrochloride (AL3818) Drug-Drug Interaction Study in Healthy Volunteers” NCT07438886 ↗ “Other Name: AL3818” NCT03778853 ↗ |
| Known as | ALC | “Anlotinib (ALC) is administered at 12mg/d QD,day1\~14, 21d/cycle.” NCT06506838 ↗ |
| Known as | Allotinib | “Allotinib (AL3818) is manufactured by Zhengda Tianqing Pharmaceutical Group Co., LTD. (CTTQ; Lianyungang, Jiangsu, China) self-developed TKI drugs” NCT06429397 ↗ |
| Known as | ALTN | “Anlotibib (ALTN) is a kind of innovative medicines approved by State Food and Drug Administration(SFDA) which was researched by Jiangsu Chia-tai Tianqing Pharmaceutical Co., Ltd.” NCT01878448 ↗ |
| Known as | Anlootinib hydrochloride | “Anlootinib hydrochloride is a multi-target tyrosine kinase inhibitor that has shown good efficacy in solid tumors such as NSCLC, ovarian cancer, soft tissue tumors, and...” NCT04223583 ↗ |
| Known as | Anlotinib | “This phase 1b/2 study evaluates the safety and efficacy of AL3818 (anlotinib) hydrochloride in combination with Opdivo (nivilumab) for the treatment patients with of...” NCT04165330 ↗477“Anlotinib is a multi-target tyrosine kinase inhibitor that can target and inhibit vascular endothelial growth factor receptor (VEGFR), fibroblast growth factor receptor (FGFR),...” NCT07142421 ↗ “Non-squamous NSCLC: almonertinib (110 mg/d) plus anlotinib (12mg/d) is started on the first day of each treatment cycle and administered every three weeks until disease...” NCT06043973 ↗ “Sintilimab 200 mg intravenously on day 1, pegaspargase 2500 IU/m² on day 1 with a maximum single dose of 3750 IU, and anlotinib 8 mg orally on days 1-14, repeated every 21 days...” NCT07678229 ↗ “Efficacy and Safety of Ensartinib Combined With Anlotinib in Lorlatinib-Resistant ALK-Positive Non-small Cell Lung Cancer(NSCLC): An Exploratory Analysis” NCT07671560 ↗ “Thus, our study aimed to evaluate the efficacy and safety of a new regimen of anlotinib plus PD-1 inhibitor to treat refractory solid tumor.” PMID 37155342 ↗ May 2023 “Treatment comprised up to eight 21-day cycles of sintilimab 200 mg (day 1), pegaspargase 2500 IU/m2 (day 1), and anlotinib 8 mg (days 1-14)” PMID 41774854 ↗ Mar 2026 “Anlotinib: 8 mg orally once daily, starting on Day 1 of each cycle, taken for 2 consecutive weeks followed by a 1-week rest period.” NCT07239622 ↗ “Anlotinib Hydrochloride Combined With Whole Brain Radiotherapy for the Treatment of Brain Metastases in Small Cell Lung Cancer” NCT06611657 ↗ “Antiangiogenesis targeted drugs: Bevacizumab or Anlotinib Hydrochloride, according to the standard dose treatment.” NCT06878625 ↗ “treated with irinotecan (50 mg/m2/d d1-5 Q3W) in combination with Anlotinib (12 mg Qd, 2 weeks on and 1 week off)” PMID 38310286 ↗ Feb 2024 |
| Known as | Anlotinib dihydrochloride | ChEMBL registry synonym — accepted as the source's own label CHEMBL4303201 ↗ |
| Known as | Anlotinib hydrochloride | “Anlotinib Hydrochloride is a multi-target receptor tyrosine kinase inhibitor with significant inhibitory activity against angiogenesis related kinases (VEGFR1/2/3, FGFR1/2/3,...” NCT04611711 ↗62“Anlotinib hydrochloride is a multi-target receptor tyrosine kinase inhibitor that has significant inhibitory activity against angiogenesis related kinases such as VEGFR1/2/3,...” NCT04684017 ↗ “Anlotinib hydrochloride, a novel oral multitarget tyrosine kinase inhibitor, has significant inhibitory activity against angiogenesis-related kinases, such as VEGFR, FGFR,...” PMID 37580661 ↗ Aug 2023 “Anlotinib hydrochloride is a novel oral tyrosine kinase inhibitor (TKI) targeting vascular endothelial growth factor receptor (VEGFR), fibroblast growth factor receptor (FGFR),...” NCT05539118 ↗ “The purpose of this study is to evaluate the efficacy and safety of Benmelstobart Injection combined with Anlotinib Hydrochloride and chemotherapy as first-line treatment for...” NCT07510594 ↗ “Anlotinib hydrochloride capsules: 10mg once a day, oral before breakfast, continuous administration for 14 days, discontinuation for 7 days, that is, 21 days (3 weeks) as a...” NCT05736952 ↗ “Anlotinib hydrochloride is a muti-target tyrosine kinase inhibitor that inhibits both tumor angiogenesis and tumor cell proliferation by blocking VEGFR, FGFR, PDGFR, and c-Kit...” NCT06062563 ↗ “Patients receive neoadjuvant therapy with oral anlotinib hydrochloride capsules and intravenous benmelstobart injection, followed by partial nephrectomy for localized renal...” NCT07627464 ↗ “Anlotinib Hydrochloride: Administered orally at a dose of 10 mg daily, taken for 2 consecutive weeks followed by 1 week off, in repeated 3-week (21-day) cycles.” NCT07849712 ↗ “Anlotinib hydrochloride capsules: Capsule; specifications 12mg; oral, once a day, every 12mg, continuous medication two weeks after 1 week deactivated.” NCT04620837 ↗ “Anlotinib Hydrochloride Capsule: Oral on an empty stomach, once a day, 1 capsule each time, orally for 2 consecutive weeks, stop for 1 week” NCT04671303 ↗ |
| Known as | Anlotinib hydrochloride capsule | “Anlotinib hydrochloride capsule 12mg given orally in fasting conditions, once daily in 21-day cycle (14 days on treatment from Day 1-14, 7 days off treatment from Day 15-21)” NCT04439890 ↗3“Anlotinib hydrochloride capsule 12mg given orally in fasting conditions, once daily in 21-day cycle” NCT05494060 ↗ “Anlotinib hydrochloride capsule: oral administration, once daily(QD) ;” NCT05068206 ↗ “Drug: Anlotinib Hydrochloride Capsule” NCT05549973 ↗ |
| Known as | Anlotinib Hydrochloride Capsules | “Anlotinib Hydrochloride Capsules (12 mg orally, once daily before breakfast; CTTQ, Lianyungang, Jiangsu, China), Toripalimab (240 mg intravenously, once every 3 weeks; Shanghai...” NCT04718701 ↗3“Anlotinib Hydrochloride Capsules: 12mg, administered on the 1-14th day of each cycle, once a day, about half an hour before breakfast (the time of daily administration should...” NCT05800080 ↗ “Anlotinib hydrochloride capsules is a new type of small molecule multi-target tyrosine kinase inhibitor against angiogenesis.” NCT04888546 ↗ “Anlotinib Hydrochloride Capsules, 12mg/d” NCT03950518 ↗ |
| Known as | Catequentinib (AL3818, Anlotinib) Hydrochloride | “Catequentinib (AL3818, Anlotinib) Hydrochloride” NCT05612191 ↗ |
| Known as | Catequentinib dihydrochloride | ChEMBL registry synonym — accepted as the source's own label CHEMBL4303201 ↗ |
| Known as | Catequentinib Hydrochloride | “A Phase III Study of AL3818 (Anlotinib, Catequentinib) Hydrochloride Monotherapy in Subjects With Metastatic or Advanced Alveolar Soft Part Sarcoma, Leiomyosarcoma and Synovial Sarcoma” NCT03016819 ↗2“A Study of Catequentinib Hydrochloride (AL3818) in Endometrial, LGSOC, STS or GBM Cancers” NCT07811297 ↗ “Catequentinib Hydrochloride (AL3818) Drug-Drug Interaction Study in Healthy Volunteers” NCT07438886 ↗ |
| Known as | Focus V | “Jiangsu Chia-Tai Tianqing Pharmaceutical and Advenchen Laboratories are co-developing anlotinib (Focus V®) for the treatment of advanced cancer.” PMID 29943374 ↗ Jul 2018 |
| Known as | Hydrochloride anlotinib | “Hydrochloride anlotinib is a small molecular anti-angiogenesis drug with multiple targets.” NCT04772001 ↗1“Hydrochloride anlotinib is a small molecular anti-angiogenesis drug with multiple targets.” NCT05772377 ↗ |
| Action | Inhibit | “ALTN is a kinase inhibitor of receptor tyrosine with multi-targets” NCT01874873 ↗2“Vascular endothelial growth factor receptor 2 inhibitor” CHEMBL4303201 ↗ “Vascular endothelial growth factor receptor 3 inhibitor” CHEMBL4303201 ↗ |
| Modality | Small molecule | “ALTN is a kinase inhibitor of receptor tyrosine with multi-targets, especially for VEGFR2 and VEGFR3.” NCT01878448 ↗ |
| Route | Oral | “oral medicine.” NCT01833923 ↗ |
| Target | CYP3A4 | “Catequentinib hydrochloride is a strong Cytochrome enzyme P450 3A4 (CYP3A4) inhibitor” NCT03016819 ↗ |
| Target | FLT4 | “Vascular endothelial growth factor receptor 3 inhibitor” CHEMBL4303201 ↗ |
| Target | KDR | “Vascular endothelial growth factor receptor 2 inhibitor” CHEMBL4303201 ↗ |