Shed will manage patient acquisition, clinical operations, and platform delivery, while LTR Pharma supplies the intranasal technology. ROXUS aims to capture market share from traditional oral medications by offering a delivery system that can trigger results in as little as five minutes. According to LTR Pharma’s Phase II interim clinical data, the treatment demonstrated a median Tmax of 10 minutes following administration.
Morley Baker, CEO of Shed and Mavrox, identified the product as a rare innovation in a stagnant category. The company has already opened an early-access waitlist on the Mavrox website to gauge consumer interest ahead of the formal rollout. While the product is being marketed as a significant shift in erectile dysfunction care, the companies note that ROXUS remains a compounded prescription medication and has not yet received formal U.S. Food and Drug Administration approval. Patients will be required to undergo a clinical evaluation by a licensed provider before gaining access to the treatment.




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