Autopsy report · NCT06456567
A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-2)
Cause of deathFunding or business
“Sponsor business decision”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 3
- Sponsor
- Vor Biopharma
- Sponsor type
- Industry
- Conditions
- Systemic Lupus Erythematosus
- Interventions
- Telitacicept; Placebo
- Participants
- 0
- Sites
- 4
- Countries
- United States
Trials that died the same way
- Study of Vitespen (HSPPC-96, Oncophage ®) for Immune Response Assessment in Participants With Resectable Renal Cell Carcinoma at Intermediate Risk of Recurrence
“Sponsor's business decision” - Study With Bispecific Antibody Engaging T-cells, in Patients With Progressive Cancer Diseases With Positive PSCA Marker
“business decision by sponsor” - Efficacy and Safety of Using MPC-5971 in Subjects Undergoing Shock Wave Lithotripsy
“Sponsor Corporate Business Decision” - A Phase 1a/1b Study of ACTM-838 in Patients With Advanced Solid Tumors
“Sponsor's strategic business decision” - Nab-Paclitaxel/STI-3031 Complex (AP160-Complex) for the Treatment of Advanced or Metastatic Solid Tumors
“Sponsor business considerations”
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.