Autopsy report · NCT05140824
A Study to Evaluate the Safety, Tolerability, and PK Profile of Single and Multiple Doses TJ202 in Patient With Systemic Lupus Erythematosus
Cause of deathFunding or business
“Company development strategy adjustment”
Life of this trial
- Registered 2 months before it started.
- Ran for about 11 months before it stopped.
- 1 participant enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- TJ Biopharma Co., Ltd.
- Sponsor type
- Industry
- Conditions
- Systemic Lupus Erythematosus (SLE)
- Interventions
- Placebo; TJ202 injection
- Participants
- 1
- Sites
- 2
- Countries
- China
Trials that died the same way
- Study of SIM0501 Alone and in Combination in Patients With Advanced Solid Tumors
“Company development strategy change” - IBI397 or Combination Therapies in Patients With Advanced Malignancies
“Due to the company's development strategy adjustment” - A Study of OVV-01 Injection in Combination With IBR900 Cell Injection in Patients With Advanced Malignant Tumors
“Research and development strategy adjustment” - Evaluation of Safety and Efficacy of Dehydrated Human Amnion-Intermediate-Chorion Membrane (dHAICM) Allograft in Treatment of Partial Thickness Thermal Burns
“Change in company strategy.” - A Clinical Investigation to Assess the Effectiveness of Benzocaine Condoms in Healthy Adult Men
“Change of the product development strategy”
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.