Pharmaceutical Business review

Chroma receives IND approval from FDA

UK-based Chroma said that it will shortly start its second phase II trial, in non-small cell lung cancer (NSCLC). This follows the recent initiation of a phase II trial for this drug in acute myeloid leukaemia.

The approval was based on a phase I study for the drug which showed one partial responder and six patients with confirmed stable disease of at least three months duration, out of a total of 41 patients treated with a variety of doses of the drug, Chroma said. The drug was well-tolerated during the study and drug exposure was consistent with the proposed once-daily oral dosing.

Ian Nicholson, CEO of Chroma, said: “We are pleased to have met this major milestone with the approval of Chroma's first IND application and to be entering our second phase II clinical trial. We believe the phase I data demonstrates this new agent could be used for the treatment of a number of solid tumors, including NSCLC, a patient group which has substantial unmet medical need.”