EU application withdrawn for Balimek in NRAS-mutant melanoma.

Pierre Fabre Médicament officially notified the Committee for Medicinal Products for Human Use (CHMP) that it wished to withdraw its application for a marketing authorisation for Balimek (binimetinib), for the treatment of melanoma. Balimek was expected to be used for treating melanoma (a type of skin cancer) that had spread or could not be removed by surgery. It was to be used in patients who had a specific genetic mutation (change) called NRAS Q61 mutation.

The company presented data from one main study comparing Balimek with dacarbazine (a cancer medicine used for treating melanoma). The study involved 402 patients with advanced melanoma with the NRAS Q61 mutation that had spread or could not be removed by surgery. The main measure of effectiveness was how long patients lived without their disease getting worse. Based on the data reviewed, at the time of the withdrawal, the CHMP had some concerns and was of the provisional opinion that Balimek could not have been approved for the treatment of advanced melanoma in patients with the NRAS Q61 mutation. The CHMP noted that patients treated with Balimek lived slightly longer without their disease getting worse compared with those receiving dacarbazine. Considering this, along with data on the time patients lived overall and their quality of life, the CHMP considered that Balimek's effectiveness was questionable.

Moreover, the CHMP was concerned that Balimek was linked to worse side effects than dacarbazine.The Committee also considered that although no medicine is approved specifically to treat patients with the NRAS Q61 mutation, there are effective treatments for melanoma in general. The evidence provided was insufficient to show that Balimek fulfils an unmet medical need.Therefore, at the time of the withdrawal, the CHMP was of the opinion that the benefits of Balimek did not outweigh its risks. In its letter notifying the Agency of the withdrawal of the application, the company stated that the withdrawal is based on CHMP’s opinion that the data supplied did not provide sufficient evidence to conclude that the medicine’s benefits outweigh its risks.