A 12-Week Placebo-Controlled Study to Investigate the Efficacy, Safety, and Tolerability of RO7017773 in Participants Aged 15-45 Years With Autism Spectrum Disorder (ASD)

PHASE2CompletedINTERVENTIONAL
Enrollment

104

Participants

Timeline

Start Date

March 31, 2021

Primary Completion Date

May 15, 2024

Study Completion Date

May 15, 2024

Conditions
Autism Spectrum Disorder (ASD)
Interventions
DRUG

Placebo

Participants will receive oral placebo for approximately 12 weeks.

DRUG

RO7017773

Participants will receive oral RO7017773 for approximately 12 weeks.

Trial Locations (21)

10461

Montefiore Medical Center, The Bronx

10962

Nathan Kline Institute, Orangeburg

15203

UPMC Western Psychiatric Institute and Clinic, Pittsburgh

16147

Ist. G. Gaslini, Genoa

23842

Istituto Scientifico Medea, Bosisio Parini (LC)

28009

Hospital General Universitario Gregorio Marañon, Madrid

32803

APG- Advanced Psychiatric Group, Orlando

37212

Vanderbilt Medical Center, Nashville

43210

Ohio State University, Columbus

44106

University Hospitals, Cleveland

60612

Rush University Medical Center, Chicago

85006

Southwest Autism Research and Resource Center, Phoenix

95123

P.O. Gaspare Rodolico, Catania

06519-1124

Yale University / Yale-New Haven Hospital, New Haven

55414-2959

University of Minnesota, Minneapolis

V1Y 1Z9

Okanagan Clinical Trials, Kelowna

A1B 3V6

Janeway Childrens Health, St. John's

M4G 1R8

Holland Bloorview Kids Rehabilitation Hospital, East York

N6A 4G5

London Health Sciences Centre, London

08007

IGAIN (Instituto Global de Atención Integral al Neurodesarrollo), Barcelona

08035

Hospital Universitari Vall d'Hebron, Barcelona

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT04299464 - A 12-Week Placebo-Controlled Study to Investigate the Efficacy, Safety, and Tolerability of RO7017773 in Participants Aged 15-45 Years With Autism Spectrum Disorder (ASD) | Biotech Hunter | Biotech Hunter