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Northstrive Biosciences Seeks FDA Guidance for Novel Muscle-Preserving Obesity Treatment EL-22

7 months ago2 min read

Key Insights

  • Northstrive Biosciences has submitted a pre-IND meeting request to FDA for EL-22, an innovative myostatin-targeting probiotic designed to preserve muscle mass during weight loss treatment.

  • The company aims to discuss the combination therapy of EL-22 with GLP-1 receptor agonists for obesity treatment, with FDA response expected in Q1 and potential meeting in Q2.

  • Following regulatory guidance, Northstrive plans to file an IND application in 2025 to commence clinical trials evaluating EL-22's efficacy in preventing muscle loss during GLP-1 agonist-based obesity treatment.

Northstrive Biosciences has taken a significant step forward in addressing a critical challenge in obesity treatment by submitting a pre-Investigational New Drug (pre-IND) meeting request to the FDA for their novel therapeutic candidate, EL-22. This innovative treatment aims to tackle the common issue of muscle loss associated with weight reduction therapies.

Novel Approach to Muscle Preservation During Weight Loss

EL-22 represents a groundbreaking approach in obesity treatment, utilizing an engineered probiotic designed to express myostatin on its surface. This patent-pending technology specifically targets the myostatin pathway, which plays a crucial role in muscle health regulation. The development comes at a critical time when concerns about muscle mass preservation during aggressive weight loss treatments have gained increasing attention in the medical community.

Strategic Development Timeline and Regulatory Path

The company anticipates receiving the FDA's response to their pre-IND meeting request within the first quarter. If granted, a formal meeting will be scheduled for Q2 2024, where Northstrive Biosciences will seek the agency's guidance on two critical aspects:
  • The adequacy of completed nonclinical studies
  • Proposed clinical development plans for EL-22 in combination with GLP-1 receptor agonists
Following successful regulatory discussions, Northstrive Biosciences has outlined plans to submit a full IND application in 2025, which would pave the way for clinical trials evaluating EL-22's effectiveness when combined with GLP-1 receptor agonists in overweight or obese patients.

Combination Therapy Strategy

The company's approach focuses on developing EL-22 as a complementary treatment to be administered alongside GLP-1 receptor agonists, which have emerged as a leading class of obesity medications. This combination strategy aims to address one of the key limitations of current weight loss treatments by potentially preserving muscle mass while patients undergo weight reduction therapy.
The development of EL-22 represents a potential paradigm shift in obesity treatment, offering a novel solution to the challenge of maintaining muscle health during weight loss interventions. As the obesity treatment landscape continues to evolve, innovations like EL-22 could play a crucial role in optimizing patient outcomes by addressing multiple aspects of weight management simultaneously.
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Sources

PMGC it has schedules a pre-IND meeting with FDA for EL-22

markets.businessinsider.comMar 10, 2025

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