Simultaneously, the company has requested the FDA for fast track designation for Actimmune. The company also intends to commence a Phase III trial in the second quarter of
As part of the deal, Lonza will manufacture material for the Phase III trial of Cx601 in the US at Lonza’s cell therapy production facility in Walkersville, US.
In September 2014, the company reported positive results from a Phase II trial of MOB-015. The new patent includes composition of matter claims directed to a new topical
Recently, the company started a Phase I clinical trial evaluating the combination of VS-5584 and VS-6063 to treat patients with relapsed or progressive malignant pleural mesothelioma. The combination
Under the deal, PATH will provide funding to support product development, preclinical testing and manufacturing, with the goal to qualify and select a final development candidate to advance
The multicenter, dose-escalation Phase I trial is designed to evaluate the safety and tolerability of ALRN-6924 as a single agent. ALRN-6924 is a potent and specific re-activator of
A total of 15 patients aged two to 18 years from two groups were included in this pediatric-specific extension trial. The first group included ten previously treatment-naïve pediatric
The US Food and Drug Administration (FDA) has already granted clearance for the company’s investigational new drug (IND) submission and Phase II trial associated with Boxaban oral capsule.
ADXS-HPV is Advaxis’s investigational Lm-LLO immunotherapy designed to treat human papillomavirus (HPV)-associated cancers, while epacadostat is Incyte’s investigational oral indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor. As part of the
The company said that three hospitals in the Philippines are expected to join the Phase II trial. Philippines is the 19th country to approve the company’s Phase III
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