Autopsy report · NCT05160168
A Study of THE-630 in Patients With Advanced Gastrointestinal Stromal Tumors (GIST)
Cause of deathSafety, also funding or business
“The Sponsor terminated the study due to early dose-limiting toxicities.”
Life of this trial
- Registered 1 month before it started.
- Ran for about 2 years 1 month before it stopped.
- 32 participants enrolled.
- Results were posted on the registry 4 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- Theseus Pharmaceuticals
- Sponsor type
- Industry
- Conditions
- Gastrointestinal Stromal Tumors (GIST); Neoplasms, Connective Tissue; Neoplasms, Connective and Soft Tissue; Neoplasms by Histologic Type; Neoplasms; Gastrointestinal Neoplasms
- Interventions
- THE-630
- Participants
- 32
- Sites
- 7
- Countries
- United States
Trials that died the same way
- Safety and Efficacy Evaluation of Bosutinib Plus Atezolizumab in Newly Diagnosed Chronic Leukemia Adult Patients
“The study has been prematurely terminated due to the onset of 2 dose limiting toxicities in 2 patients.” - Safety Study of Bevacizumab (Avastin) With Thoracic Radiation in Non-small Cell Cell Lung Cancer
“Study terminated due to toxicity” - Evaluation of Apricoxib (Selective Cyclooxygenase 2 Inhibition) in Modulating T Regulatory Cells of Patients With Early Stage Non-small Cell Lung Cancer
“Drug sponsor stopped drug manufacture due to toxicity issues from other studies” - An Evaluation of the Erchonia Laser As a Non-Invasive Treatment to Improve the Appearance of Skin Laxity
“The study was terminated early due to sponsor decision unrelated to safety or efficacy findings” - A Phase II Study of Belinostat in Combination With Bortezomib in Patients With Relapsed, Refractory Multiple Myeloma
“Terminated due to dose limiting toxicity”
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.