Drugs / Sonesitatug Vedotin

Trials 8

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT04805307 Dec 2020 → Apr 2024 gastric carcinoma, malignant pancreatic neoplasm Keymed Biosciences Co.Ltd Completed No outcome recorded
Phase 25 trials
Phase 2 NCT07143604 Aug 2025 → Aug 2026 overdue gastric cancer, gastroesophageal junction adenocarcinoma AstraZeneca Active not recruiting No outcome recorded
Phase 2 NCT07069712 Jul 2025 → Nov 2027 expected gastroesophageal adenocarcinoma AstraZeneca Recruiting No outcome recorded
Phase 2 NCT06630130 Jan 2025 → Oct 2028 expected gastric cancer Jeeyun Lee Recruiting No outcome recorded
Phase 2 NCT06219941 Dec 2023 → Nov 2026 expected biliary tract cancer, gastric cancer, gastroesophageal junction adenocarcinoma, pancreatic ductal adenocarcinoma AstraZeneca Recruiting No outcome recorded
Phase 2 NCT05702229 Jan 2023 → Nov 2027 expected gastric cancer AstraZeneca Recruiting No outcome recorded
Phase 32 trials
Phase 3 NCT07431281 Feb 2026 → Aug 2029 expected esophageal cancer, gastric cancer, gastroesophageal junction adenocarcinoma AstraZeneca Recruiting No outcome recorded
Phase 3 NCT06346392 Mar 2024 → May 2026 overdue gastric adenocarcinoma, gastroesophageal junction adenocarcinoma AstraZeneca Active not recruiting Mixed

News releases announcing trial results or a regulatory action · 4

DateIssuerRelease
2026-07-28 Keymed Biosciences Co.Ltd Results CLDN18.2 ADC CMG901:首个全球范围III期取得积极顶线结果,总生存期获益显著 keymedbio.com ↗
CLARITY-Gastric01全球III期临床试验公布的积极顶线结果显示,与研究者选择的治疗方案相比,CMG901在二线及后线CLDN18.2阳性晚期胃癌患者中展现出具有统计学显著性且极具临床意义的OS改善。
2026-07-27 AstraZeneca Results Sonesitatug vedotin demonstrated a statistically significant and highly clinically meaningful improvement in overall survival in 2nd and later-line CLDN18.2-positive advanced gastric/GEJ cancers astrazeneca.com ↗
2024-02-24 Keymed Biosciences Co.Ltd Results 疗效优异:靶向Claudin 18.2抗体偶联药物CMG901 I期临床研究最新数据亮相ASCO年会 keymedbio.com ↗
研究结果显示,CMG901具有良好的安全性和耐受性,在治疗晚期Claudin 18.2高表达胃癌/胃食管结合部腺癌受试者中表现出了优秀的疗效
2023-07-24 Keymed Biosciences Co.Ltd Results CMG901 I期临床研究数据最新结果在ASCO Plenary Series以口头报告形式公布 keymedbio.com ↗
89例可评估的Claudin 18.2阳性胃癌或胃食管结合部腺癌患者在三个剂量组的确认的客观缓解率(ORR)为33%,确认的疾病控制率(DCR)为70%。

Evidence & citations 9 cited values

Every value below carries the sentence it was read from. 10 sources stand behind the page.

FieldValueCited text
Known as Sonesitatug vedotin ClinicalTrials.gov intervention name — accepted as the source's own label NCT07431281 ↗
2

NCT06630130 ↗

NCT07069712 ↗

Known as AZD0901 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07143604 ↗
3

NCT05702229 ↗

NCT06219941 ↗

NCT06346392 ↗

Known as CMG901 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04805307 ↗
Known as Sone-Ve “Sonesitatug Vedotin(Sone-Ve) 2.2mg /kg IV on D1, Q3W for 3 cycles” NCT06630130 ↗
Known as Sonesitatug vedotina ChEMBL registry synonym — accepted as the source's own label CHEMBL6068297 ↗
Known as Sonesitatug vedotine ChEMBL registry synonym — accepted as the source's own label CHEMBL6068297 ↗
Modality Other / unclassified “an anti Claudin18.2 ADC; IV infusion” NCT05702229 ↗
Route Intravenous “CMG901 will be administered intravenously (IV) on Day 1 of every 21-day cycle.” NCT04805307 ↗
Target CLDN18 “Claudin 18.2-targeting antibody-drug conjugate CMG901” PMID 39788133 ↗ Jan 2025