Autopsy report · NCT05154630
Study on Tolerability and Pharmacokinetics of TQB2858 Injection in Subjects With Advanced Malignant Tumors
Cause of deathFunding or business
“The sponsor has decided to terminate this study based on the current clinical research status of dual antibody drugs and full communication with the investigators.”
Life of this trial
- Registered 1 month before it started.
- Ran for about 1 year 6 months before it stopped.
- 8 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
- Sponsor type
- Industry
- Conditions
- Advanced Cancer; Advanced Soft-tissue Sarcoma
- Interventions
- TQB2858 injection
- Participants
- 8
- Sites
- 5
- Countries
- China
Trials that died the same way
- Safety and Efficacy of MAGE-A3/A6 T Cell Receptor Engineered T Cells (KITE-718) in HLA-DPB1*04:01 Positive Adults With Advanced Cancers
“The study was terminated due to the sponsor's decision to discontinue the clinical trial.” - Study of Magrolimab Combinations in Patients With Relapsed/Refractory Multiple Myeloma
“This study was terminated early due to the Sponsor's decision to discontinue development of the investigational drug and close the program.” - Study of Melflufen (Melphalan Flufenamide) in Combination With Daratumumab in Relapsed-Refractory Multiple Myeloma
“The sponsor decided to terminate the study due to financial issues following an FDA request for a partial clinical hold.” - A Study of GFH312 in Patients With Peripheral Artery Disease (PAD) and Intermittent Claudication (IC)
“The study was terminated by sponsor for reasons of adjusted clinical development strategy.” - Phase II Study of TAEST16001 in Soft Tissue Sarcoma
“The study was terminated due to initiation of a new clinical trial with an updated study design.”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.