Phase Ⅰ Study to Evaluate the Safety and Tolerability of Using F520
Phase Ⅰ Study to Evaluate the Safety and Tolerability of Using F520 by Advanced Tumor Subjects
Sponsor: Shandong New Time Pharmaceutical Co., LTD
This PHASE1 trial investigates Advanced Solid Tumor,Recurrent Solid Tumor,Lymphoma,Recurrent Lymphocyte Depleted Classical Hodgkin Lymphoma and is currently ongoing. Shandong New Time Pharmaceutical Co., LTD leads this study, which shows 8 recorded versions since 2019 — indicating limited longitudinal coverage. As an oncology study, it adds to the longitudinal record of treatment development for this indication.
Status Flow
Change History
8 versions recorded-
Sep 2024 — Present [monthly]
Unknown PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Unknown PHASE1
Status: Unknown Status → Unknown
-
Nov 2022 — Jul 2024 [monthly]
Unknown Status PHASE1
Status: Recruiting → Unknown Status
-
Jan 2021 — Nov 2022 [monthly]
Recruiting PHASE1
-
Nov 2020 — Jan 2021 [monthly]
Recruiting PHASE1
▶ Show 3 earlier versions
-
Apr 2020 — Nov 2020 [monthly]
Recruiting PHASE1
-
May 2019 — Apr 2020 [monthly]
Recruiting PHASE1
Status: Not Yet Recruiting → Recruiting
-
Oct 2018 — May 2019 [monthly]
Not Yet Recruiting PHASE1
First recorded
Eligibility Summary
No eligibility information available.
Contact Information
- Shandong New Time Pharmaceutical Co., LTD
For direct contact, visit the study record on ClinicalTrials.gov .