TQB3122
/ Sino Biopharm
- LARVOL DELTA
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January 29, 2026
A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of TQB3122 Capsules in Subjects With Advanced Malignant Tumors
(clinicaltrials.gov)
- P1 | N=86 | Recruiting | Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Not yet recruiting ➔ Recruiting
Enrollment open • First-in-human • Breast Cancer • Oncology • Ovarian Cancer • Solid Tumor
December 09, 2025
A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of TQB3122 Capsules in Subjects With Advanced Malignant Tumors
(clinicaltrials.gov)
- P1 | N=86 | Not yet recruiting | Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
New P1 trial • Oncology • Solid Tumor
August 11, 2025
APPLICATION FOR CLINICAL TRIAL OF TQB3122 “PARP1 INHIBITOR” ACCEPTED BY NMPA
(Sino Biopharm Press Release)
New trial • Solid Tumor
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