GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

Oteseconazole overview

Oteseconazole (Vivjoa) is a potent and selective anti fungal agent. It is formulated as hard gelatin capsules for oral route of administration, Vivjoa is indicated to reduce the incidence of recurrent vulvovaginal candidiasis (RVVC) in females with a history of RVVC who are not of reproductive potential.

Oteseconazole (VT-1161) is under development for the treatment of fungal diseases such as Coccidioidomycosis, cryptococcal meningitis, recurrent vulvovaginal candidiasis, Rhizopus oryzae infection causes zygomycosis, onychomycosis and chronic mucocutaneous candidiasis. It is a small molecule. The drug candidate is administered through oral route as a tablet. It acts by targeting lanosterol 14-alpha-demethylase or CYP51. The drug candidate is based on Metallophile technology platform. It was also under development for the treatment of athlete's foot (tinea pedis) and Coccidioidomycosis.

Mycovia Pharmaceuticals overview

Mycovia Pharmaceuticals (Mycoyia Pharmaceuticals) formerly known as Viamet Pharmaceuticals Inc, discovers and develops novel medicinal drugs based on metalloenzyme chemistry and biology technology platform. Its product portfolio includes clinical-stage compounds such as VT-1161, an oral inhibitor used for the treatment of onychomycosis and recurrent vulvovaginal candidiasis; VT-1129, an oral agent for the treatment of cryptococcal meningitis; VT-1598, an oral inhibitor to treat invasive fungal infections, including coccidioidomycosis. The company’s proprietary MIDAS technology (Metalloenzyme Inhibitor Design and Synthesis) enables to discover metalloenzyme inhibitors that target fungal CYP51 of both chronic and life threatening fungal infections. Mycoyia Pharmaceuticals is headquartered in Durham, North Carolina, the US.

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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.

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