Highlights
X4 Pharmaceuticals receives breakthrough therapy designation from FDA for Mavorixafor to t
Mavorixafor is a potential first-in-class, once-daily, oral, small molecule antagonist of chemokine receptor CXCR4, a
Boehringer, Eli Lilly begin sixth phase III study for Jardiance in heart failure
The Empulse, which is the sixth phase III study in the Jardiance heart failure programme, will evaluate whether in-ho
Roche’s risdiplam meets primary endpoint in phase 3 SMA trial
Risdiplam has been designed to be a survival motor neuron-2 (SMN2) splicing modifier. The drug works by durably incre
NEC and VAXIMM announce collaboration to advance personalized neoantigen cancer vaccines
NEC Corporation (NEC; TOKYO: 6701), a leader in IT and network technologies, and VAXIMM AG, a Swiss/German biotech co
New Bespoke service for small and emerging Pharma and Biotech companies
A new, tailor-made service for small and emerging Pharma and Biotech companies has just been launched by specialist scie
US FDA accepts regulatory submission for Selumetinib
This is the first acceptance of a regulatory submission for an oral MEK 1/2 monotherapy for patients with NF1, a rare
EpicentRx closes $35m series D financing to support development of small molecule immunoth
The purpose of this funding round, which will be split into three tranches, is to progress the late-stage clinical de
Shionogi gets FDA approval for cUTI drug Fetroja
Fetroja has been approved for patients 18 years of age or older who have limited or no alternative treatment options
Alkermes to buy Rodin Therapeutics for up to $950m
As per the terms of the deal, Rodin’s security holders will secure an upfront cash payment of $100m upon comple
Novartis’ Adakveo approved by FDA to reduce VOCs in sickle cell disease
Formerly known as SEG101, Adakveo has been approved for reducing the incidents of vaso-occlusive crises (VOCs), or pa
The Medicines Company announces that the ORION-10 study of inclisiran showed durable and p
In ORION-10, twice-yearly dosing with inclisiran sodium 300 mg met all primary and secondary efficacy endpoints, was
Qtrilmet approved in EU to treat type-2 diabetes
The approval is based on data from five Phase III trials which evaluated combinations of Forxiga (dapagliflozin) and