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83 Fulton St. , Boonton, NJ, 07005, US
How to Ensure Your CDMO Partner Has the Experience and Expertise to Get Your HPAPI Product Across the Finish Line.
Released By Enteris BioPharma
CDMO operations are housed within a 32,000-square-foot, FDA-inspected and cGMP-compliant facility in northern New Jersey.
Data indicates that the formulation delivers comparable or greater drug levels than subcutaneous or depot injection.
By: Charlie Sternberg
Third milestone payment related to the development of Oral KORSUVA.
By: Tim Wright
Removing API supply as a criterion in the “Go/No-Go” decision tree and enhancing the opportunity to successfully navigate the pharmaceutical “Valley of Death.”
By: thomas daggs
Also launches CDMO business for the development and manufacture of difficult to formulate drugs and highly potent compounds.
Cara has a non-exclusive, royalty-bearing license to the Peptelligence technology to develop, manufacture and commercialize Oral KORSUVA
By: Kristin Brooks
Will develop an oral formulation of a peptide-based injectable therapeutic
Enters agreement with Nordic Bioscience to lead the formulation and clinical manufacturing of Peptelligence-enabled compounds
35-year industry vet, Joel Tune, will take the company helm
Why nimble niche CMOs may be a better choice
By: paul shields
CMOs, CDMOs and CROs are becoming more specialized to stand out in a hyper competitive market
Will offer production of API using microbial expression systems
Saxon to license Peptelligence platform
By: Gil Roth
Zietsman, Mehta, and Shields join executive team
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