Afamelanotide (Scenesse, Clinuvel Pharmaceuticals) is a linear MC1R selective tridecapeptide, approved by the FDA on October 8, 2019, and by the EMA on December 22, 2014, exclusively for the treatment of erythropoietic protoporphyria (EPP) in adults
Retatrutide, however, wont be on the market until it completes Phase 3 and earns FDA approval
An anti-ASCT2 monoclonal antibody suppresses gastric cancer growth by inducing oxidative stress and antibody dependent cellular toxicity in preclinical models
the human retinal pigment epithelial cell line, assessing its potential to reduce intracellular inflammation
You start at 0.25 mg once weekly for four weeks, primarily to assess tolerability