Merck unveils first human data for Alzheimer’s candidates
The company also revealed that MK-2214 has received Fast Track Designation from the U.S. Food and Drug Administration
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
Agreement adds a new preclinical ADC with potential for enhanced anti-tumour activity and best-in-class profile
MKP11093 has shown strong results in preclinical studies with a promising safety and selectivity profile
CGX-926 is the first clinical candidate addressing MC4R-deficient genetic obesity
Inclacumab was generally well tolerated in THRIVE-131
The use of Apisolex polymer excipient has been proven to increase the solubility of certain APIs by as much as 50,000-fold
SIM0500 is a humanized trispecific antibody that targets GPRC5D, BCMA, and CD3
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