Autopsy report · NCT05148195
A Phase II Study of Envofolimab and BD0801 With/Without Chemotherapy in Patients With Advanced Solid Tumors
Cause of deathFunding or business
“The study was terminated due to the sponsor's research and development strategy adjustment.”
Life of this trial
- Registered 1 month before it started.
- Ran for about 1 year 7 months before it stopped.
- 86 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Jiangsu Simcere Pharmaceutical Co., Ltd.
- Sponsor type
- Industry
- Conditions
- Advanced Solid Tumor
- Interventions
- Envofolimab; BD0801; Docetaxel; Irinotecan; Leucovorin calcium; 5-Fluorouridine
- Participants
- 86
- Sites
- 24
- Countries
- China
Trials that died the same way
- 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.” - A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunogenicity of LB4330 in Patients With Advanced Solid Tumors(MEETCD8-001)
“Due to adjustments in the sponsor's development strategy, it has been decided to terminate the study.” - Long-term, Non-interventional, Observational Study Following Treatment With Fate Therapeutics FT500 Cellular Immunotherapy
“This study was terminated by the Sponsor.” - A Study of AC682 In Chinese Patients With ER+/HER2- Locally Advanced or Metastatic Breast Cancer
“Voluntarily terminate the study since the sponsor's development strategy was adjusted.” - A Study to Assess Recurrence of Actinic Keratosis in Participants Treated With Methyl Aminolevulinate Hydrochloride Cream or Vehicle Cream Who Achieved Complete Response to Treated Lesions in Earlier Study
“The study was terminated early as per Sponsor's decision”
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.