Aurigene, Alveus advance obesity pipeline with ALV-200 candidate nomination
The collaboration combines Alveus’ expertise in metabolic biology and therapeutic strategy with Aurigene’s integrated discovery capabilities
The collaboration combines Alveus’ expertise in metabolic biology and therapeutic strategy with Aurigene’s integrated discovery capabilities
The drug also showed a manageable safety profile, with just 6.4% of patients stopping treatment due to side effects. No new safety concerns emerged
The protections extend through at least 2035, with the potential for further extensions
MYC, a master regulator of oncogenic transcription, drives multiple high-burden cancers but has long eluded direct pharmacologic control
Applications include detailed scientific rationale and supporting clinical evidence
The company also revealed that MK-2214 has received Fast Track Designation from the U.S. Food and Drug Administration
Pfizer and Valneva have been collaborating on VLA15’s development and commercialization since April 2020
The Fast Track Designation was supported by nonclinical data as well as clinical results from the ongoing Phase I/IIa trial evaluating the safety and tolerability
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