Agomab receives FDA Fast Track Designation for AGMB-129 in Fibrostenosing Crohn’s Disease and starts STENOVA Phase 2a clinical trial
Agomab Therapeutics NV (‘Agomab’) today announced that it received Fast Track Designation from the U.S. Food and Drug Administration (FDA) for AGMB-129 for the potential treatment of Fibrostenosing Crohn’s Disease (FSCD). In addition, Agomab has initiated its STENOVA Phase 2a clinical trial evaluating AGMB-129, an oral gastro-intestinal (GI)-restricted small molecule inhibitor of ALK5 (TGF-βRI or ALK5), in patients with symptomatic FSCD.
Fibrotic strictures develop in nearly 50% of patients living with Crohn’s disease and remain a major therapeutic challenge as strictures are the main cause for bowel surgery, an outcome which occurs in approximately 75% of Crohn’s disease patients. The TGF-β pathway is a key driver of fibrosis in the GI tract, and inhibition through its receptor ALK5 is considered the most effective therapeutic approach to block it.
AGMB-129 is the first drug candidate to receive FDA Fast Track Designation for the treatment of Fibrostenosing Crohn’s Disease. Fast Track Designation is intended to expedite the development and review of new therapies that treat serious or life-threatening conditions for which there is an unmet medical need. To qualify, available clinical and non-clinical data needs to demonstrate the potential to address the unmet medical need. Benefits of Fast Track Designation include the opportunity for frequent meetings with the FDA to discuss trial design, development plans and data needed to support drug approval; the ability to submit a New Drug Application (NDA) on a rolling basis; and eligibility for priority review.
The STENOVA Phase 2a clinical trial is a randomized, double-blind, placebo-controlled study in 36 patients with symptomatic FSCD. Patients will be randomized to receive one of two doses of AGMB-129 or a placebo for 12 weeks. The multi-center study is global with investigational sites in the USA, Canada and Europe. The primary endpoints are the safety and tolerability of AGMB-129 in FSCD patients. Secondary endpoints include the pharmacokinetics and target engagement at the site of the ileal strictures.
“The start of this Phase 2a clinical study is an important milestone in the development of AGMB-129. Intestinal strictures cause severe obstructive symptoms, are thought to induce the formation of fistulae, and are the main cause of bowel surgery. Receiving the first FDA Fast Track Designation in fibrostenosing Crohn’s disease indicates that the FDA acknowledges the severity and unmet medical need in this indication,” said Philippe Wiesel, Chief Medical Officer at Agomab Therapeutics. “We look forward to working with investigators as well as the regulators to develop AGMB-129 in this particularly severe disease for which there is no approved therapy.”
“Intestinal strictures remain the major therapeutic challenge in patients with Crohn’s disease. Because available anti-inflammatory agents have limited efficacy on strictures, direct anti-fibrotic therapies are needed,” commented Florian Rieder, MD, Vice-Chair Department of Gastroenterology, Hepatology and Nutrition, Cleveland Clinic, Cleveland, OH, and co-lead of the STAR consortium, a network of academic and industry partners which aims to advance the development of new agents for FSCD. “The initiation of a Phase 2a trial with a potent anti-fibrotic agent as well as the Fast Track Designation represent a very exciting milestone for patients with Fibrostenosing Crohn’s Disease.”
AGMB-129 is an investigational drug and not approved by any regulatory authority. Its efficacy and safety have not been established.