Breast cancer drug 'will likely be approved' by FDA

27 January 2017

According to a new evidence review, PB272 (neratinib), which is currently under review by the US Food and Drug Administration (FDA), will “...likely be approved for the extended adjuvant treatment of HER2-positive early stage breast cancer.”

The report from Advera Health Analytics collates data from 11 clinical trials to assess the candidate breast cancer therapy in comparison with Herceptin (trastuzumab) and Tykerb (lapatinib).

PB272 is being developed by USA-based Puma Biotechnology (Nasdaq: PBYI). Herceptin is sold by Swiss giant Roche (ROG: SIX) and Tykerb (known as Tyverb in Europe) is sold by British firm GlaxoSmithKline (LSE: GSK).

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