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NCT05306574 · ClinicalTrials.gov registry record · Phase 3

A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-1)

A Phase 3 study, sponsored by Vor Biopharma.

Terminated
Registry status
Phase 3
Development phase
91
Enrollment target

NCT05306574: Clinical Trial Phase 3 study, sponsored by Vor Biopharma.

NCT05306574 is a Phase 3 study that was terminated before completion, run by Vor Biopharma. The registered enrollment target is 91 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05306574, a Phase 3 study, was terminated before completion, sponsored by Vor Biopharma.

TERMINATED
Registry status
Phase 3
Development phase
91 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the efficacy and safety of telitacicept in the treatment of moderately to severely active SLE.

Primary Outcome

Proportion of subjects achieving an SLE Responder Index (SRI-4) response at Week 52

Interventions

  • BIOLOGICAL Placebo
  • BIOLOGICAL Telitacicept

Trial Details

FieldValue
Enrollment Target 91 participants
Start Date 2022-06-20
Est. Completion 2025-01-06
Phase Phase 3
Vor Biopharma

6 total trials

Why NCT05306574 stopped before completion

NCT05306574 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 91 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT05306574 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05306574 about?

NCT05306574 is a clinical study titled "A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-1)". The purpose of this study is to evaluate the efficacy and safety of telitacicept in the treatment of moderately to severely active SLE.

What is the current status of trial NCT05306574?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 91 participants. The study started on 2022-06-20. Estimated completion is 2025-01-06.

What interventions are being tested in trial NCT05306574?

The interventions under investigation include: Placebo (BIOLOGICAL), Telitacicept (BIOLOGICAL).

Who is sponsoring clinical trial NCT05306574?

This trial is sponsored by Vor Biopharma, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05306574's enrollment target sits among peer trials

91 1724th of 2000 higher than 277 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05306574, the US trial registry maintained by the National Library of Medicine. NCT05306574 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.