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ACTIVE NOT RECRUITING Phase 2

A Study of Efficacy and Safety of Rosnilimab in Subjects with Moderate to Severe Rheumatoid Arthritis (RENOIR)

NCT06041269 · View on ClinicalTrials.gov ↗

Study Summary

RENOIR Study: This study will evaluate the safety, tolerability, and efficacy of Rosnilimab in subjects with moderate to severe Rheumatoid Arthritis (RA)

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Rosnilimab

Study Locations (20)

Florida

  • AnaptysBio Investigative Site 10-103 — Aventura
  • AnaptysBio Investigative Site 10-141 — Avon Park
  • AnaptysBio Investigative Site 10-118 — Boynton Beach
  • AnaptysBio Investigative Site 10-125 — Daytona Beach
  • AnaptysBio Investigative Site 10-122 — Homestead
  • Anaptys Bio Investigative Site 10-142 — Miami
  • AnaptysBio Investigative Site 10-140 — Miami
  • AnaptysBio Investigative Site 10-102 — Miami
  • AnaptysBio Investigative Site 10-124 — Plantation

California

  • AnaptysBio Investigative Site 10-105 — Covina
  • Anaptys Bio Investigative Site 10-119 — Rancho Mirage
  • AnaptysBio Investigative Site 10-113 — San Diego
  • AnaptysBio Investigative Site 10-127 — San Francisco
  • AnaptysBio Investigative Site 10-136 — Temecula
  • AnaptysBio Investigative Site 10-133 — Upland
  • AnaptysBio Investigative Site 10-112 — Whitter

Arizona

  • AnaptysBio Investigative Site 10-132 — Flagstaff
  • AnaptysBio Investigative Site 10-130 — Glendale
  • AnaptysBio Investigative Site 10-129 — Phoenix
  • AnaptysBio Investigative Site 10-131 — Tucson

Trial Details

FieldValue
Enrollment Target 420 participants
Start Date 2023-08-31
Est. Completion 2025-05-30
Phase Phase 2

Sponsor

AnaptysBio

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06041269

The ClinicalTrials.gov registry entry for NCT06041269 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 420 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AnaptysBio, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Rheumatoid Arthritis appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06041269 reports 20 study locations spanning 3 distinct geographic areas — top geographies include Florida, California, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06041269 about?

NCT06041269 is a clinical study titled "A Study of Efficacy and Safety of Rosnilimab in Subjects with Moderate to Severe Rheumatoid Arthritis (RENOIR)". RENOIR Study: This study will evaluate the safety, tolerability, and efficacy of Rosnilimab in subjects with moderate to severe Rheumatoid Arthritis (RA)

What is the current status of trial NCT06041269?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 420 participants. The study started on 2023-08-31. Estimated completion is 2025-05-30.

What conditions does trial NCT06041269 study?

This clinical trial studies the following conditions: Rheumatoid Arthritis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06041269?

The interventions under investigation include: Placebo (DRUG), Rosnilimab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06041269?

This trial is sponsored by AnaptysBio, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06041269 being conducted?

This trial has 20 study locations across Arizona, California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial