Basilea Pharma: FDA Allows To Proceed With Phase 1 Study For BAL0891

(RTTNews) - Basilea Pharmaceutica Ltd. (BPMUF.PK) announced the FDA has approved the company's Investigational New Drug application for the kinase inhibitor BAL0891. This allows the company to initiate the phase 1 clinical study in the first quarter of 2022. The IND approval triggers a milestone payment of 1.85 million Swiss francs to NTRC, from which Basilea in-licensed BAL0891.

Laurenz Kellenberger, Chief Scientific Officer of Basilea, said: "The drug candidate offers the potential for a targeted development strategy in multiple cancers. We are looking forward to adding this potential first-in-class mitotic checkpoint inhibitor to our clinical oncology pipeline."

The views and opinions expressed herein are the views and opinions of the author and do not necessarily reflect those of Nasdaq, Inc.

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