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Study identifier: NCT06840496 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

To Investigate the Efficacy of Treatment With Oral NA-921 (Bionetide) Versus Placebo in Females With Rett Syndrome

Condition: Rett Syndrome  ·  Sponsor: Biomed Industries, Inc.

PhasePhase 3
Planned participants210
Who can joinFemale, 5 Years to 20 Years
Healthy volunteersNo

About this study

Primary Objective • To investigate the efficacy of treatment with oral Bionetide versus placebo in girls and women with Rett syndrome Key Secondary Objective • To investigate the efficacy of treatment with oral Bionetide versus placebo on ability to communicate in girls and women with Rett syndrome

This description comes directly from the study's public registry record.

Talk to the study team

David L Nguyen, PhD  ·  1-800-824-5135  ·  research@biomedind.com

Jennifer Thomposn, MS  ·  1-800-824-5135  ·  research@biomedind.com

Always discuss trial participation with your own doctor first.

Locations (18)

Biomed Testing Facility # BIO-01-85012Phoenix, Arizona, United StatesRecruiting
Biomed Testing Facility # BIO-05-92093La Jolla, California, United StatesRecruiting
Biomed Testing Facility # BIO-04-90095Los Angeles, California, United StatesRecruiting
Biomed Testing Facility # BIO-03-95817Sacramento, California, United StatesRecruiting
Biomed Testing Facility # BIO-02-94104San Francisco, California, United StatesRecruiting
Biomed Testing Facility #BIO-06-80042Aurora, Colorado, United StatesRecruiting
Biomed Testing Facility #BIO-07-33606Tampa, Florida, United StatesRecruiting
Biomed Testing Facility #BIO-08-60612Chicago, Illinois, United StatesRecruiting
Maryland Locations Biomed Testing Facility #BIO-9-21205Baltimore, Maryland, United StatesRecruiting
Biomed Testing Facility #BIO-10-02115Boston, Massachusetts, United StatesRecruiting
Biomed Testing Facility #BIO-13-10467The Bronx, New York, United StatesRecruiting
Biomed Testing Facility #BIO-17-19104Philadelphia, Pennsylvania, United StatesRecruiting

+ 6 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06840496