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155b Commerce Drive , Hauppauge, NY, 11788, US
Renejix is the leading end to end CDMO accelerator for small molecule oral dosage forms at a competitive price. We have produced over 200 FDFs, 5+ billion dosages annually, and have a staff of ~500 employees. Take your molecules from concept to commercialization in record time by cutting 20 weeks off early and late phase timelines!
The collaboration aims to advance the discovery and development of novel oral candidates.
By: Charlie Sternberg
Provides intelligent packaging for precise therapy monitoring of syringes used in clinical trials.
OncoACP3 is a small molecule ligand with high affinity and specificity for Acid Phosphatase 3 (ACP3), a novel target in prostate cancer.
The companies partner on antibody drug conjugates, drug substance, and drug product manufacturing services.
By: Rachel Klemovitch
Partnership includes joint research, technology transfer, and co-development of lead candidates.
Becomes a fully integrated front- and back-end company, offering the full biomanufacturing workflow, from discovery and development to manufacture and supply.
Approved for the detection and localization of prostate-specific membrane antigen (PSMA)-positive lesions in adults with prostate cancer.
Robert will be responsible for creating commercial and organizational synergies between the API Solutions and CDMO operations.
Supports late-stage development and scalable manufacturing for LP-310
Released By Mikart
Addressing increasing complexity, cost of drug development, and navigating regulatory compliance.
By: Kristin Brooks
Montagut brings more than 25 years of senior leadership experience in the pharmaceutical sector.
The CDMO's head of development talks about ADCs, accelerated timelines, and the push for end-to-end development services.
By: Tim Wright
This project could reduce costs in pharmaceutical development and manufacturing.
Will add further sterile fill/finish capacity over the course of the next year.
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