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Filler G, Amendt P, von Bredow MA, Rohde W, Ehrich JH (1998) Slowly deteriorating insulin secretion and C-peptide production characterizes diabetes mellitus in infantile cystinosis
A realistic timeline, based on where the Phase 3 programme is now, looks like this: FDA submission in the U.S.: late 2026 or 2027 FDA approval: 2027 or 2028 UK MHRA review: typically 12 to 24 months after FDA approval NHS access through a NICE appraisal: a separate process, usually 12 to 24 months after MHRA approval The earliest UK private access through online pharmacies, mirroring how Mounjaro and Wegovy first launched here, is likely 2027 or 2028
What do you think about the role of real-time monitoring in improving postoperative care
Earlier in the diabetes treatment progression
Essentially, the FDA has not formally evaluated this exact mixture for safety/efficacy, but each ingredients effects are well-known
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