Press Releases June 1, 2026 08:00 AM

MBX Biosciences to Host Virtual Investor Event to Discuss Once-Weekly Canvuparatide Presentations at ENDO 2026

MBX Biosciences to present Phase 2 trial data for once-weekly canvuparatide at ENDO 2026 and host investor webcast

By Maya Rios MBX

MBX Biosciences announced it will present new Phase 2 and one-year extension data on its once-weekly canvuparatide treatment for chronic hypoparathyroidism at the Endocrine Society's Annual Meeting (ENDO 2026). The company will also host an investor webcast to discuss the clinical trial results, highlighting progress toward Phase 3 development.

MBX Biosciences to Host Virtual Investor Event to Discuss Once-Weekly Canvuparatide Presentations at ENDO 2026
MBX

Key Points

  • Presentation of one-year open-label extension data and 12-week Phase 2 trial results for once-weekly canvuparatide at ENDO 2026.
  • Scheduled investor webcast and conference call with company management and scientific advisors to discuss clinical progress.
  • Canvuparatide targets chronic hypoparathyroidism and the company is advancing other metabolic disorder therapies, impacting the biotech and pharmaceutical sectors.

CARMEL, Ind., June 01, 2026 (GLOBE NEWSWIRE) -- MBX Biosciences, Inc. (Nasdaq: MBX), a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of novel precision peptide therapies for the treatment of endocrine and metabolic disorders, today announced that it will host an investor webcast and conference call at 8:00 am ET on Friday, June 12, 2026 to discuss presentations for once-weekly canvuparatide at the upcoming Endocrine Society’s Annual Meeting (ENDO 2026) in Chicago.

One-year open-label extension (OLE) data from the Phase 2 trial of once-weekly canvuparatide will be presented at the 3rd Parathyroid Summit during ENDO 2026 on Friday, June 12, 2026. Full results from the 12-week AvailTM Phase 2 trial of once-weekly canvuparatide will be presented in an oral presentation at ENDO 2026 at 3:00 pm CT on Saturday, June 13, 2026.

The Company will host a conference call and webcast at 8:00 am ET on Friday, June 12, 2026 to discuss full results from the 12-week AvailTM Phase 2 trial and one-year OLE data for once-weekly canvuparatide. Company management will be joined by Richard DiMarchi, Ph.D., Distinguished Professor of Chemistry at Indiana University and MBX scientific co-founder, and Michael T. Collins, M.D., endocrinologist and Senior Clinical Advisor at the National Institutes of Health. Those who would like to participate may access the live webcast here or dial 1-877-407-0779 (US) or 1-201-389-0914 (international). The live and archived webcast of the call and slide presentation will be available in the Investors section of the Company’s website at https://investors.mbxbio.com/news-events/events.

About MBX Biosciences
MBX Biosciences is a biopharmaceutical company focused on the discovery, development and commercialization 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 preparing for Phase 3 development; and an obesity portfolio that includes MBX 4291 in Phase 1 development and MBX 5765 in preclinical development, as well as additional discovery candidates. The Company is based in Carmel, Indiana and Burlington, Massachusetts. To learn more, please visit the company website at www.mbxbio.com and follow it on LinkedIn.

Media Contact:
George Shea
We. Communications
[email protected]
(937) 232-4889

Investor Contact:
Jim DeNike
MBX Biosciences
[email protected]


Risks

  • Clinical trial data may not meet expectations or regulatory approval standards, affecting future development and commercialization.
  • Competitive landscape in endocrine and metabolic disorder therapies could impact market share and profitability.
  • Dependence on successful Phase 3 development and regulatory approvals introduces inherent uncertainties in biopharmaceutical markets.

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