Drugs / GC101
last change Nov 2025 re-read 3 minutes ago

GC101

Gene therapy (AAV / viral vector) targets SMN1

Developed for
spinal muscular atrophy · spinal muscular atrophy, type II · spinal muscular atrophy, type III
Investigated by
GeneCradle Inc

Trials 4

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/23 trials
Phase 1/2 NCT06421831 May 2024 → Dec 2026 expected spinal muscular atrophy, type III GeneCradle Inc Recruiting No outcome recorded
Phase 1/2 NCT05901987 Aug 2023 → Apr 2025 overdue spinal muscular atrophy, type II GeneCradle Inc Active not recruiting No outcome recorded
Phase 1/2 NCT05824169 Feb 2023 → Dec 2026 expected spinal muscular atrophy GeneCradle Inc Recruiting No outcome recorded
Phase 31 trial
Phase 3 NCT06971094 May 2025 → Dec 2026 expected spinal muscular atrophy GeneCradle Inc Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 10

DateIssuerRelease
2025-11-06 Shanghai Juncell Therapeutics Results SITC 2025 | 单次静脉回输,4周后高级别脑胶质瘤清零 juncell.com ↗
回输后仅4 周,影像学显示其脑部肿瘤被完全清除,疗效评估为完全缓解(CR),后续再无复发,至今维持无瘤生存状态已超20个月。
2025-07-18 Shanghai Juncell Therapeutics Results 首例转组患者成功PR,GC101努力惠及每个受试者 juncell.com ↗
回输后 6 周的首次疗效评估,整体靶病灶缩小达到 31.9% ,其中 62mm 的最大单病灶缩小近 40% ,总体疗效达到 PR 。
2025-06-20 Shanghai Juncell Therapeutics Results 18cm靶病灶PR,GC101治疗后线肢端恶黑患者显奇效 juncell.com ↗
回输 18 周后,整体影像评价为 部分缓解(PR) 。
2025-03-12 Shanghai Juncell Therapeutics Results 病灶消除,GC101 TIL疗法使KRAS突变肺癌患者持续获益 juncell.com ↗
第 12 周靶病灶 CR , 18 周时 CR 仍维持。
2024-12-13 Shanghai Juncell Therapeutics Results 又双叒!肺癌患者肿瘤大幅缩小 juncell.com ↗
在接受 GC101 TIL 治疗后的首次肿瘤评估显示,多病灶明显缩小,整体缩小 33% ,达到部分缓解( PR ),其中脾脏转移灶缩小 44% 。
2024-12-09 Shanghai Juncell Therapeutics Results KRAS突变肺癌患者肿瘤快速缩小 juncell.com ↗
近日,一位KRAS G12D 突变的 NSCLC 患者在回输君赛生物 GC101 TIL 后的首次肿瘤评估,肿瘤整体缩小 45% ,达到部分缓解 (PR) 。
2024-12-05 Shanghai Juncell Therapeutics Regulatory 获批关键II期临床,君赛GC101 TIL疗法更安全、更优效 juncell.com ↗
近日,君赛生物宣布, GC101 TIL 注射液 首个关键性 II 期注册临床试验 已获得国家药品监督管理局药品审评中心 (CDE) 批准,用于经 PD-1 抗体治疗进展或不耐受的晚期黑色素瘤患者 (NCT06703398) 。
2024-05-23 Shanghai Juncell Therapeutics Results 无需IL-2给药,创新TIL疗法的临床结果首发国际权威杂志 juncell.com ↗
经TIL细胞回输治疗,未观察到与细胞相关的严重不良反应;5例患者(35.7%)达到客观缓解,3例患者达到完全缓解,且长期持续。
2023-04-08 Shanghai Juncell Therapeutics Results 「新闻」无需高强度清淋化疗、无需IL-2给药,君赛生物TIL GC101临床Ⅰ期试验安全性良好,已现客观疗效! juncell.com ↗
目前,该受试者经单次输注TIL细胞(低剂量组,5e9)治疗后已完成二次评估,靶病灶缩小超过30%,达到PR疗效,且持续缓解中。
2022-04-24 Shanghai Juncell Therapeutics Regulatory 「新闻」君赛生物首款TIL细胞新药获得NMPA临床试验默示许可 juncell.com ↗
2022年4月24日,上海君赛生物科技有限公司(以下简称君赛生物)自主开发的首款TIL细胞药物“自体天然肿瘤浸润淋巴细胞注射液(GC101 TIL)”(受理号:CXSL2200070)正式获得国家药品监督管理局(NMPA)的临床试验默示许可。

All press releases naming this drug 13 releases

DateIssuerRelease

Evidence & citations 4 cited values

Every value below carries the sentence it was read from. 4 sources stand behind the page.

FieldValueCited text
Known as GC101 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06421831 ↗
3

NCT06971094 ↗

NCT05824169 ↗

NCT05901987 ↗

Modality Gene therapy (AAV / viral vector) “Self-complementary AAV9 carrying a codon-optimized SMN coding sequence(coSMN1) driven by CMV enhancer and chicken β-actin promoter” NCT05824169 ↗
Route Intrathecal “GC101 will be administrated intrathecally.” NCT05824169 ↗
Target SMN1 “Self-complementary AAV9 carrying a codon-optimized SMN coding sequence(coSMN1) driven by CMV enhancer and chicken β-actin promoter” NCT05824169 ↗