A Study With TEPEZZA in Patients With Diffuse Cutaneous Systemic Sclerosis (dcSSc)

PHASE1TerminatedINTERVENTIONAL
Enrollment

3

Participants

Timeline

Start Date

November 17, 2021

Primary Completion Date

November 29, 2022

Study Completion Date

December 8, 2022

Conditions
Diffuse Cutaneous Systemic Sclerosis
Interventions
BIOLOGICAL

TEPEZZA

TEPEZZA is a fully human anti-IGF-1R mAb. TEPEZZA will be provided in single-dose 20 mL glass vials as a freeze-dried powder. Each vial of TEPEZZA must be reconstituted with 10 mL of water for injection. Reconstituted TEPEZZA solution must be further diluted in 0.9% (w/v) sodium chloride (NaCl) solution prior to administration. TEPEZZA will be administered in 100 mL or 250 mL infusion bags (100 mL infusion bags for doses up to 1800 mg and 250 mL infusion bags for doses \> 1800 mg).

OTHER

Placebo

Placebo will consist of normal saline (0.9% NaCl) solution and will be administered in 100 mL or 250 mL infusion bags, as would be appropriate, per weight-based dosing volumes (100 mL infusion bags for doses up to 1800 mg and 250 mL infusion bags for doses \> 1800 mg).

Trial Locations (7)

21224

The Johns Hopkins Bayview Medical Center, Baltimore

43614

University of Toledo Medical Center, Toledo

44195

The Cleveland Clinic, Cleveland

77030

UT Physicians Center for AutoImmunity, Houston

90045

Pacific Arthritis Care Center, Los Angeles

900095-1670

UCLA Division of Rheumatology, Los Angeles

06473

Yale North Haven Medical Center, New Haven

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY

NCT04478994 - A Study With TEPEZZA in Patients With Diffuse Cutaneous Systemic Sclerosis (dcSSc) | Biotech Hunter | Biotech Hunter