Leveraging our proprietary IMG-1 polypeptide, Progenalen Pro Peptide is a professional-grade, once-daily supplement designed to help support: - Healthy glucose metabolism* - Metabolic wellness and cellular aging* - Fat metabolism and cardiovascular health support* - Convenient dosing via an advanced liquid-filled Licap capsule This launch reflects years of research into how IMG-1 can support the bodys regenerative processes, with the goal of extending healthy function across systems

Key facts for understanding the device context: Trial structure: Four or more core trials (TRIUMPH-1 through TRIUMPH-4 plus TRIUMPH-Outcomes), enrolling 5,800 or more participants across programs Administration: Subcutaneous injection, once weekly, dose escalation to 12mg maximum TRIUMPH-4 results (December 2025): Participants on 12mg retatrutide lost an average of 28.7% body weight at 68 weeks, versus 2.1% on placebo (Giblin et al., PMID 41090431) Phase 2 comparison: 24.2% body weight loss at 48 weeks on 12mg (Jastreboff et al., NEJM 2023) - a different trial, shorter duration, earlier data TRIUMPH-Outcomes: Active Phase 3 trial (NCT06383390), estimated 10,000 participants, completion February 2029 - investigating cardiovascular outcomes What the Phase 3 Device Disclosure Gap Means Eli Lilly has not disclosed pen device specifications for retatrutide because the drug is not yet approved, and device details are part of the commercial product launch package

Durand CM, Perroy J, Loll F, Perrais D, Fagni L, Bourgeron T, et al
A more detailed assessment score than NDS is the Neuropathy Impairment Score (NIS), which evaluates: muscle strengthtested in eight muscle groups through flexion and extension, scored from 0 to 4, where 0 is normal and 4 indicates no activity and sensitivity and reflexesincludes vibration, touch, sharp stimulus and position sense
Ozempic approved to reduce cardiovascular risk Ozempic (semaglutide 0.5 mg, 1 mg, and 2 mg) previously received FDA approval for cardiovascular health in people with type 2 diabetes after combined results from the SUSTAIN-6 and PIONEER-6 trials showed a 24% reduction in major adverse cardiac events (MACE) such as heart attack, stroke, and other cardiovascular-related deaths