Autopsy report · NCT05226507
A Phase 1 Clinical Study of NXP800 in Subjects With Advanced Cancers and Expansion in Subjects With Ovarian Cancer
Cause of deathFunding or business
“Study terminated due to various reasons impacting the feasibility of future clinical development”
Life of this trial
- Ran for about 3 years before it stopped.
- 45 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- Nuvectis Pharma, Inc.
- Sponsor type
- Industry
- Conditions
- Advanced Solid Tumor; Ovarian Cancer; Ovarian Clear Cell Carcinoma; Ovarian Clear Cell Tumor; Ovarian Clear Cell Adenocarcinoma; Ovarian Endometrioid Adenocarcinoma
- Interventions
- NXP800
- Participants
- 45
- Sites
- 22
- Countries
- United Kingdom, United States
Trials that died the same way
- A Long Term Safety Study of Mavrilimumab in Adult Subjects With Rheumatoid Arthritis
“The study was terminated after approximately 3 years due to future clinical development plans, including ethical considerations.” - 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.” - Relative Bioavailability Study of Ropinirole Implants in Parkinson's Patients on L-Dopa Switched From Oral Ropinirole
“This study was terminated for reasons not related to efficacy or safety” - A Dose Exploration Study With Birabresib (MK-8628) in Participants With Selected Hematologic Malignancies (MK-8628-005)
“This study was terminated due to limited efficacy and not due to safety reasons” - 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.