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Injectable semaglutide delivers nearly 100% of the dose to your system, while oral formulations achieve only 0.4% to 1.5% bioavailability without special absorption enhancers

Translarna (Ataluren, New Molecular Entity) Developer: PTC Therapeutics Modality: Small Molecule PDUFA Date: February or March 2025 Indication/Description: Central nervous system disorders / Treatment for Duchenne muscular dystrophy (nmDMD) with nonsense mutations Review Type: Priority Review Submission Date: August to September 2024 Omvoh (Mirikizumab-MRKZ) Developer: Eli Lilly Modality: Monoclonal Antibody PDUFA Date: No later than February 2025 Indication/Description: Gastrointestinal diseases / New indication for Omvoh, for treating moderate to severe active Crohn's disease in adults Review Type: Standard Review Submission Date: March to April 2024 Enhertu (Fam-Trastuzumab Deruxtecan-NXKI) Developer: Daiichi Sankyo/AstraZeneca Modality: ADC (Antibody-Drug Conjugate) PDUFA Date: February 1, 2025 Indication/Description: Cancer / New indication for Enhertu, for treating unresectable or metastatic HER2-low or HER2 ultra-low breast cancer in adults Review Type: Priority Review Submission Date: August 1, 2024 Review Status: FDA accepted the application on October 1, 2024

Use Sterile Water for Injection (SWFI) or Bacteriostatic Water (BAC) per your labs SOP for precise dosing

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Marys Hospital who presented the AIBIS data, described PG-102 as a program built for vulnerable patients, seeking clinically meaningful glucose lowering while preserving metabolic resilience. Kim made the same point more bluntly in his remarks, warning that for some patients weight loss is really undesirable, including leaner patients and older adults at risk of sarcopenia