Randomized, Blinded Discontinuation Trial of Ocrelizumab in Early Relapsing Multiple Sclerosis (AMS05)

Status: Recruiting
Location: See all (11) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This study is a prospective, multi-center, randomized, double blinded, placebo-controlled study of OCR treatment-discontinuation in patients with early RMS. All eligible participants will be initiated on OCR using the standard approved administration schedule of two 300 mg infusions separated by 14 days (i.e., Days 0 and 14) for a total of 600 mg, followed by 600 mg infusions at Month 6,12, 18, and 24. At Month 24, participants will be randomized (2:1) to one of two Arms with randomized treatment beginning at Month 30: Arm 1: placebo infusions every 6 months; or Arm 2: OCR infusions every 6 months. The treatment period will be for a total of 48 months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 55
Healthy Volunteers: f
View:

• Have at least one clinical episode that satisfies McDonald 2017 criteria for early Multiple sclerosis (MS) for up to 2 years post-event with a dissemination in time that can be met clinically, by Magnetic Resonance Imaging (MRI), or based on oligoclonal band (OCB) positivity

• Have a length of disease duration, from first symptom, of ≤ 2 years

• For women of childbearing potential: Agreement to remain abstinent (refrain from heterosexual intercourse) or use effective methods of contraception during the treatment period and for at least 6 months after the last dose of study drug:

‣ A woman is considered to be of childbearing potential if she is postmenarcheal, has not reached a postmenopausal state (≥12 continuous months of amenorrhea with no identified cause other than menopause), and has not undergone surgical sterilization (removal of ovaries and/or uterus)

⁃ Examples of contraceptive methods include bilateral tubal ligation, male sterilization, established hormonal contraceptives that inhibit ovulation, hormone- releasing intrauterine devices, and copper intrauterine devices

⁃ The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the participant. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or post ovulation methods) and withdrawal are not acceptable methods of contraception

⁃ Barrier methods must always be supplemented with the use of a spermicide

Locations
United States
Connecticut
Yale School of Medicine
RECRUITING
New Haven
Washington, D.c.
MedStar Georgetown University Hospital
RECRUITING
Washington D.c.
Massachusetts
Massachusetts General Hospital
RECRUITING
Boston
University of Massachusetts Memorial Medical Center
RECRUITING
Worcester
New York
Icahn School of Medicine at Mount Sinai
RECRUITING
New York
University of Rochester Medical Center
RECRUITING
Rochester
Oklahoma
Oklahoma Medical Research Foundation
RECRUITING
Oklahoma City
Pennsylvania
University of Pennsylvania, Perelman School of Medicine
RECRUITING
Philadelphia
Texas
University of Texas Southwestern Medical Center
RECRUITING
Dallas
The University of Texas Health Science Center at Houston, McGovern Medical School
RECRUITING
Houston
Virginia
Virginia Commonwealth University School of Medicine
RECRUITING
Richmond
Contact Information
Primary
Amit Bar-Or
(215) 316-5151
Time Frame
Start Date: 2023-01-12
Estimated Completion Date: 2030-11-01
Participants
Target number of participants: 123
Treatments
Experimental: Ocrelizumab Arm
All eligible participants will be initiated on OCR using the standard approved administration schedule of two 300 mg infusions separated by 14 days (i.e., Days 0 and 14) for a total of 600 mg, followed by 600 mg infusions at Month 6, 12, 18, and 24.~In this arm participants will continue to receive OCR infusions every 6 months through Month 48.
Placebo_comparator: Placebo Arm
All eligible participants will be initiated on OCR using the standard approved administration schedule of two 300 mg infusions separated by 14 days (i.e., Days 0 and 14) for a total of 600 mg, followed by 600 mg infusions at Month 6, 12, 18, and 24.~In this arm, starting at Month 30, participants will receive placebo infusions every 6 months through Month 48.
Sponsors
Collaborators: Autoimmunity Centers of Excellence (ACE), Genentech, Inc., Rho Federal Systems Division, Inc.
Leads: National Institute of Allergy and Infectious Diseases (NIAID)

This content was sourced from clinicaltrials.gov