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NCT05306353 · ClinicalTrials.gov registry record · Phase 2

CD40L Antagonism in Rheumatoid Arthritis (RA)

A Phase 2 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Terminated
Registry status
Phase 2
Development phase
2
Enrollment target

NCT05306353: Clinical Trial Phase 2 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT05306353 is a Phase 2 study that was terminated before completion, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 2 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05306353, a Phase 2 study, was terminated before completion, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

TERMINATED
Registry status
Phase 2
Development phase
2 participants
Enrollment target

Study Summary

The primary objective is to determine if the addition of a 12-week course of treatment with VIB4920 to TNFi treatment will result in improved clinical disease control in patients with RA who have had an inadequate response to a TNFi.

Primary Outcome

Defined by a Simplified Disease Activity Index (SDAI) \<= 11 Participants who escalate their disease-modifying therapy or take any prohibited medications for treatment of RA prior to Week 16 are considered to have failed the primary endpoint. The primary analysis will compare the primary endpoint between the two blinded study arms: VIB4920 with TNFi and VIB4920 placebo with TNFi study arms

Interventions

  • DRUG Placebo for VIB4920
  • DRUG VIB4920 with TNFi
  • DRUG VIB4920 without TNFi

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2023-07-25
Est. Completion 2025-07-28
Phase Phase 2

Why NCT05306353 stopped before completion

NCT05306353 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo for VIB4920 is the first listed.

NCT05306353 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05306353 about?

NCT05306353 is a clinical study titled "CD40L Antagonism in Rheumatoid Arthritis (RA)". The primary objective is to determine if the addition of a 12-week course of treatment with VIB4920 to TNFi treatment will result in improved clinical disease control in patients with RA who have had an inadequate response to a TNFi.

What is the current status of trial NCT05306353?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 2 participants. The study started on 2023-07-25. Estimated completion is 2025-07-28.

What interventions are being tested in trial NCT05306353?

The interventions under investigation include: Placebo for VIB4920 (DRUG), VIB4920 with TNFi (DRUG), VIB4920 without TNFi (DRUG).

Who is sponsoring clinical trial NCT05306353?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05306353's enrollment target sits among peer trials

2 2001st of 2000 the lowest of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT05306353, the US trial registry maintained by the National Library of Medicine. NCT05306353 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.