A Study to Evaluate the Safety, Tolerability and How YH002 Enters, Moves Through and Exits the Body in Subjects With Advanced Solid Malignancies
A First-in-Human (FIH), Multicenter, Open-Label, Phase 1 Dose-Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of YH002 in Subjects With Advanced Solid Malignancies
Sponsor: Eucure (Beijing) Biopharma Co., Ltd
This PHASE1 trial investigates Advanced Solid Malignancies and is currently completed. Eucure (Beijing) Biopharma Co., Ltd leads this study, which shows 9 recorded versions since 2020 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
9 versions recorded-
Sep 2024 — Present [monthly]
Completed PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE1
-
Sep 2022 — Jul 2024 [monthly]
Completed PHASE1
-
Jul 2022 — Sep 2022 [monthly]
Completed PHASE1
Status: Recruiting → Completed
-
Jun 2021 — Jul 2022 [monthly]
Recruiting PHASE1
▶ Show 4 earlier versions
-
May 2021 — Jun 2021 [monthly]
Recruiting PHASE1
-
Feb 2021 — May 2021 [monthly]
Recruiting PHASE1
Status: Not Yet Recruiting → Recruiting
-
Jan 2021 — Feb 2021 [monthly]
Not Yet Recruiting PHASE1
-
May 2020 — Jan 2021 [monthly]
Not Yet Recruiting PHASE1
First recorded
Apr 2020
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Eucure (Beijing) Biopharma Co., Ltd
For direct contact, visit the study record on ClinicalTrials.gov .