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Clinical Trials/2023-507217-10-00
2023-507217-10-00
Completed
Phase 3

A randomized, double-masked, placebo-controlled safety, tolerability, and efficacy study of VRDN-001, a humanized monoclonal antibody directed against the IGF-1 receptor, in participants with chronic thyroid eye disease (TED)

Viridian Therapeutics Inc.28 sites in 6 countries170 target enrollmentStarted: April 1, 2024Last updated:

Overview

Phase
Phase 3
Status
Completed
Sponsor
Viridian Therapeutics Inc.
Enrollment
170
Locations
28
Primary Endpoint
Overall Response Rate comprised of Proptosis Responder Rate in the most proptotic eye at 3 weeks post the fifth IV infusion and Clinical Activity Responder Rate in the most proptotic eye at 3 weeks post the fifth IV infusion.

Overview

Brief Summary

To determine the safety, tolerability, and efficacy of VRDN- 001 when given as 5 infusions of 10 mg/kg compared to placebo in participants with chronic TED.

Eligibility Criteria

Ages
18 years to 65+ years (18-64 Years, 65+ Years)
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Males and/or females of age ≥18 to ≤75 years of age and older who have a clinical diagnosis of TED with any degree of disease severity and symptoms as measured by the CAS scale (0-7).
  • Participants must have moderate to severe chronic TED with proptosis (eye bulging) of at least 3 mm and >17 mm measurement at pre-dose baseline (Day -1 or Day 1) in the study eye.
  • Have experienced eye-related symptoms or signs that began more than 15 months before study screening.
  • Must agree to use highly effective contraception as specified in the protocol.
  • Female TED participants must have a negative serum pregnancy test at Screening.

Exclusion Criteria

  • Participants who have previously received treatment with other anti-IGF-1R therapy
  • Participants who have taken corticosteroids (except topically) or selenium (except multivitamins) for any condition, including TED, within 2 weeks before starting study medication. Also exclusionary are injections of corticosteroids into the eye within 3 months prior to the first dose of study medication or having received greater than 3 injections of corticosteroids into the eye at any time.
  • Participants who have received immunosuppressive agents, radioactive iodine, any other therapy for TED, or an investigational agent for any condition within 8 weeks prior to the first dose of study medication.
  • Participants who have a decrease in disease severity and symptoms as measured by CAS scale of at least 2 points in the study eye between screening and one day before treatment, for participants who had a CAS greater than 2 at screening.
  • Participants who have a decrease of at least 2 mm in proptosis (eye bulging) in the study eye from screening to one day before treatment.
  • Participants who require immediate surgical intervention and/or have other eye conditions as evaluated by the study doctor that are not responding to treatment.
  • Female participants who are pregnant or breastfeeding.
  • Have abnormal baseline hearing assessment

Arms & Interventions

VRDN-001 (Insulin-like growth factor-1 receptor [IGF-1R] inhibitor)

Test

Intervention: VRDN-001 (Insulin-like growth factor-1 receptor [IGF-1R] inhibitor) (Drug)

SODIUM CHLORIDE

Placebo

Intervention: SODIUM CHLORIDE (Drug)

Outcomes

Primary Outcomes

Overall Response Rate comprised of Proptosis Responder Rate in the most proptotic eye at 3 weeks post the fifth IV infusion and Clinical Activity Responder Rate in the most proptotic eye at 3 weeks post the fifth IV infusion.

Overall Response Rate comprised of Proptosis Responder Rate in the most proptotic eye at 3 weeks post the fifth IV infusion and Clinical Activity Responder Rate in the most proptotic eye at 3 weeks post the fifth IV infusion.

Safety Endpoint: Adverse Events (AEs) and Serious Adverse Events (SAEs) will be monitored and recorded throughout the duration of the study. All clinically significant changes in other safety measurements will be recorded as AEs.

Safety Endpoint: Adverse Events (AEs) and Serious Adverse Events (SAEs) will be monitored and recorded throughout the duration of the study. All clinically significant changes in other safety measurements will be recorded as AEs.

Secondary Outcomes

  • Change from baseline in proptosis for the most proptotic eye at Week 15.
  • Proptosis change from baseline, general and measured by exophtalmometer and responder rate at Week 15.
  • Diplopia Responder and Resolution Rate (i.e., reduction in Diplopia Score to 0 from baseline for participants with baseline Diplopia Score >0) at Week 15.

Investigators

Sponsor
Viridian Therapeutics Inc.
Sponsor Class
Pharmaceutical company
Responsible Party
Principal Investigator
Principal Investigator

Chief Development Officer

Scientific

Viridian Therapeutics S.à.r.l.

Study Sites (28)

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