NEW YORK – Novartis' key patent on its radioligand therapy Lutathera (lutetium Lu 177 dotatate) isn't set to expire until 2038, but radiopharmaceutical company Lantheus is already preparing to ...

The agency previously declined to approve Ebvallo for Epstein-Barr virus-positive post-transplant lymphoproliferative disease and requested a new trial.

More than 30 percent of later-line patients responded to the drug in an existing Phase II trial, but some biomarker cohorts fared better.

The company's clinical development plan comprises three global Phase III studies, including two focused on infants and a third for older patients.

Waiv, previously operating as Owkin Dx, will expand global access to a pipeline of AI-driven digital pathology and multimodal tests for cancer.

The firm said it expects to file an investigational new drug application for the autologous CAR T-cell therapy TPST-2003 in the US by the end of the year.

The firm is hoping to outline a potential path to accelerated approval for SGT-003 as it gears up to launch a randomized, controlled Phase III trial.

NEW YORK – Cbio will begin a European Phase I/II trial of its autologous T-cell therapy novoleucel for patients with late-stage cervical cancer, with initial results expected by the end of the year.

The firm will use the funds, which add to the $50 million it brought in last year from stock sales, to develop its CAR-T products.

NEW YORK – The US Food and Drug Administration on Tuesday approved GSK's Wellcovorin (leucovorin calcium) as a treatment for adult and pediatric patients with cerebral folate deficiency who harbor ...

While the US Food and Drug Administration touts new regulatory flexibility for rare disease drugs, recent rejections of ...