MBX Biosciences will present findings on MBX 1416 at the American Diabetes Association’s Scientific Sessions from June 20-23, 2025.
Quiver AI Summary
MBX Biosciences, Inc., a biopharmaceutical company specializing in precision peptide therapies for endocrine and metabolic disorders, announced that it will present findings on its investigational drug MBX 1416 at the American Diabetes Association's 85th Scientific Sessions in June 2025. The drug, a glucagon-like peptide-1 receptor antagonist, showed promising results in a Phase 1 trial, demonstrating its potential to elevate and sustain blood glucose levels without weight gain, and is being developed as a treatment for post-bariatric hypoglycemia (PBH). This condition, a serious complication of bariatric surgery, leads to severe hypoglycemic episodes with no current approved therapies available. The company plans to initiate a Phase 2 trial later in 2025, as the need for effective treatments for PBH grows alongside the increasing number of bariatric surgeries. Further details on the presentations will be accessible on their publications page after the conference.
Potential Positives
- MBX Biosciences will present findings on their investigational drug MBX 1416 at the prestigious American Diabetes Association’s 85th Scientific Sessions, indicating the company's commitment to transparency and engagement with the scientific community.
- MBX 1416 shows promise as a potential treatment for post-bariatric hypoglycemia, highlighting the company's focus on addressing significant unmet medical needs in endocrine and metabolic disorders.
- The positive topline results from previous clinical trials of MBX 1416, as well as the planned Phase 2 trial, suggest ongoing progress and development in the company’s pipeline of innovative therapies.
Potential Negatives
- Although MBX 1416 shows potential, it is still in Phase 1 development, indicating that the drug is at least several years away from possible approval and market availability, which may impact investor sentiment.
- The press release emphasizes the lack of approved pharmacotherapies for post-bariatric hypoglycemia, highlighting both the medical need and the competitive landscape, suggesting potential challenges in proving the efficacy and safety of MBX 1416 against other treatment options if they emerge.
- The company may face significant scrutiny and pressure to deliver timely and effective results in its upcoming Phase 2 trial, given the complexity and seriousness of post-bariatric hypoglycemia, which could affect stakeholder confidence.
FAQ
What is MBX 1416?
MBX 1416 is an investigational long-acting GLP-1 receptor antagonist developed for treating post-bariatric hypoglycemia.
When will MBX Biosciences present its findings?
MBX Biosciences will present at the ADA's 85th Scientific Sessions from June 20-23, 2025.
What are the potential benefits of MBX 1416?
MBX 1416 aims to prevent severe hypoglycemia episodes, enhancing independence and quality of life for patients with PBH.
Is there a treatment approved for post-bariatric hypoglycemia?
No, there are currently no approved pharmacotherapies for post-bariatric hypoglycemia.
Where can I find more information about MBX Biosciences?
For more details, visit the MBX Biosciences website at https://mbxbio.com/ or their publications page.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$MBX Insider Trading Activity
$MBX insiders have traded $MBX stock on the open market 10 times in the past 6 months. Of those trades, 10 have been purchases and 0 have been sales.
Here’s a breakdown of recent trading of $MBX stock by insiders over the last 6 months:
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Full Release
CARMEL, Ind., June 10, 2025 (GLOBE NEWSWIRE) -- MBX Biosciences, Inc. (Nasdaq: MBX), a clinical-stage biopharmaceutical company focused on the discovery and development of novel precision peptide therapies for the treatment of endocrine and metabolic disorders, today announced presentations at the American Diabetes Association’s (ADA) 85th Scientific Sessions, taking place June 20-23. 2025, Chicago, IL.
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846-P - Safety, Pharmacokinetics, and Pharmacodynamics of MBX 1416, a Glucagon-Like Peptide-1 Receptor Antagonist, in Healthy Volunteers: A Phase 1 Randomized Trial
Presenter: Elisa Fabbrini, MD. PhD.
Session: General Poster Session
Date: Sunday June 22 nd , 2025
Time 12:30-1:30pm CT
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845-P - MBX 1416, a Selective GLP-1 Antagonist, Elevates and Sustains Blood Glucose in Rats without Change in Body Weight
Presenter: Richard DiMarchi, PhD.
Session: General Poster Session
Date: Sunday June 22 nd , 2025
Time: 12:30-1:30pm CT
The findings presented in the posters demonstrate the mechanism of action of MBX 1416 and illustrate its potential benefits as a once-weekly treatment for post-bariatric hypoglycemia (PBH). MBX announced earlier this year that MBX 1416 demonstrated positive topline results in a Phase 1 single ascending dose (SAD) and multiple ascending dose (MAD) clinical trial in healthy adult volunteers. A Phase 2 trial is expected to be initiated in the second half of 2025.
Following congress publication, the presentations will be available for review on MBX Biosciences publications page https://investors.mbxbio.com/news-events/presentations.
About MBX 1416
MBX 1416 is an investigational long-acting glucagon-like peptide-1 (GLP-1) receptor antagonist in development as a potential treatment for PBH. It was designed using the Company’s novel, proprietary PEP™ platform to prevent the occurrence of severe hypoglycemia in individuals with PBH so they can lead healthier and more independent lives.
About Post-bariatric Hypoglycemia
Post-bariatric hypoglycemia (PBH) is a rare and serious complication of bariatric surgery. PBH is characterized by repeated episodes of symptomatic hypoglycemia, triggered by exaggerated secretion of GLP-1 levels following a meal, and can present as early as six months after Roux-en-Y gastric bypass or sleeve gastrectomy. Hypoglycemic episodes can occur multiple times per day and can periodically manifest with severe symptoms, such as dizziness, confusion, loss of consciousness or seizure. The unpredictability of hypoglycemic episodes and their associated risks may meaningfully hinder daily activities. As a result, the patient burden can be substantial, and many individuals cannot drive, work, or live alone. To date, there are no approved pharmacotherapies to treat PBH. As the use of surgery to address metabolic conditions continues to rise, the incidence of PBH is expected to increase, reinforcing the need for safe and effective therapies.
About MBX Biosciences
MBX Biosciences is a biopharmaceutical company focused on the discovery and development of novel precision peptide therapies based on its proprietary PEP™ platform, for the treatment of endocrine and metabolic disorders. The Company is advancing a pipeline of novel candidates for endocrine and metabolic disorders with clinically validated targets, established endpoints for regulatory approval, significant unmet medical needs and large potential market opportunities. The Company’s pipeline includes canvuparatide (MBX 2109) for the treatment of chronic hypoparathyroidism (HP) in Phase 2 development; MBX 1416 for the treatment of post-bariatric hypoglycemia (PBH) in Phase 1 development; and an obesity portfolio that includes MBX 4291, with an IND filing anticipated in Q2 2025, as well as multiple discovery and pre-clinical obesity candidates. The Company is based in Carmel, Indiana. To learn more, please visit the Company website at
https://mbxbio.com/
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Media Contact:
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Investor Contact:
Jim DeNike
MBX Biosciences
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