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The agreement was reached through the Special Protocol Assessment (SPA) process. A SPA is an acknowledgement by FDA that the design and planned analysis of the Company's pivotal

Kymo Therapeutics’s ambition is to move forward Metabrain Research’s proprietary program on kynurenine metabolism (KMO) inhibitors towards clinical proof of concept, before seeking partners to complete development and

The trial is designed to evaluate the safety and efficacy of the combination in patients with refractory diffuse large B-cell lymphoma (DLBCL). PD-L1 expression in DLBCL is associated

The drug, called Zubsolv, is a formulation of buprenorphine, a semisynthetic opioid derivative of thebaine, and naloxone, an opioid overdose antidote. The new low dose, 0.7mg/0.18 mg, Zubsolv

ATTR amyloidosis disease occurs due to the deposition of transthyretin in peripheral tissues. The company said study safety monitors recommended that the phase 3 trial be stopped after

Codexis will receive an $8 million payment from Merck for completion of this milestone to be paid in the fourth quarter of 2016. Codexis President and CEO John

Solabegron is a highly potent and selective beta-3 adrenoceptor agonist that is being developed for the treatment of overactive bladder (OAB). Moreover, solabegron has already demonstrated efficacy for

Teva said the divestment of the assets and operations was part of an undertaking that it made to the European Commission related to the acquisition of Actavis Generics

Brilinta was being tested against clopidogrel in 13,885 patients in 28 countries. The study, dubbed Euclid, is the largest trial of its kind in such patients and forms