Satellos reported that it has obtained Investigational New Drug (IND) clearance from the U.S. Food and Drug Administration (FDA) and additional international regulators to initiate SAT-3247-CL-201—a three-month, randomized, double-blind, placebo-controlled Phase 2 proof-of-concept trial. The study will evaluate SAT-3247 in 51 ambulatory children diagnosed with Duchenne muscular dystrophy (Duchenne or DMD). >> Potential of SAT-3247 to Restore Muscle Regeneration in Duchenne Published in Nature
Clinical Trial of SAT-3247
- Placebo-controlled Phase 2 study will evaluate SAT-3247 treatment over three months among ambulatory children with Duchenne
- Study endpoints include safety and tolerability, effect on muscle force and function, and impact on muscle quality and regeneration
- Enrollment of first study participant anticipated by end of 2025
“We are delighted to achieve U.S. and global clearance to start our Phase 2 pediatric study of SAT-3247, which we have named BASECAMP. This important milestone positions Satellos to demonstrate the potential for SAT-3247 to safely restore the body’s ability to repair and regenerate muscle in children living with Duchenne, and to alter disease progression,” said Frank Gleeson, co-founder and CEO of Satellos. “With encouraging functional data from our Phase 1b study in adults, we have confidence in the potential for SAT-3247 to make an impact for children with Duchenne, and we are excited to begin enrollment in the trial imminently.”
In addition to the FDA clearance, the United Kingdom’s Medicine and Healthcare products Regulatory Agency (MHRA) granted authorization of the company’s Clinical Trial Application (CTA); Australia’s Human Research Ethics Committee (HREC) accepted the Therapeutic Goods Administration’s (TGA’s) Clinical Trial Notification (CTN) scheme for regulatory authorization; and the Medicines and Medical Devices Agency of Serbia (ALIMS) approved the company’s CTA. The clinical trial application is still under review in the European Union and Canada in accordance with established timelines and procedures.
SAT-3247 is an oral small-molecule therapy designed to restore the body’s ability to regenerate muscle, a process that is impaired in Duchenne. In a Phase 1a/b study in adults, SAT-3247 was safe and well-tolerated with a desirable pharmacokinetic (PK) profile. Part B of the study, composed of adults with Duchenne treated with SAT-3247 over a 28-day period, demonstrated a 118.6% mean improvement in maximum grip strength in the dominant hand and 97.9% mean improvement in the non-dominant hand, representing an approximate doubling of grip strength from ~2 kg to ~4 kg.
BASECAMP is a three-month global, randomized, double-blind, placebo-controlled, proof-of-concept study in 51 ambulatory children with Duchenne. Primary endpoints will evaluate the safety and tolerability of SAT-3247 and its effect on muscle force. Secondary endpoints will evaluate SAT-3247’s impact on muscle quality, function, and regeneration. The first participant is expected to be enrolled into the study by the end of 2025. Satellos expects to report initial interim data from BASECAMP in Q2 2026 and data from the LT-001 study in adults with DMD in Q1 2026.
About SAT-3247
SAT-3247 is a proprietary, oral, small molecule drug being developed by Satellos as a novel treatment to regenerate skeletal muscle that is lost in Duchenne muscular dystrophy and other degenerative or injury conditions. Satellos is advancing SAT-3247 as a potential treatment for DMD, independent of dystrophin and regardless of exon mutation status.
Follow This Page >>> All Clinical Trials for Duchenne
Olá como consigo inscrever meu filho nesse teste ?
Meu filho se Chama Kauê 9 anos , DMD