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Balimek is a medicine that contains the active substance binimetinib. It was to be available as tablets to be taken by mouth. Balimek was expected to be used for treating melanoma a type of skin cancer that had spread or could not be removed by surgery. These proteins encourage the growth of new cells. By blocking the MEK proteins, Balimek is expected to slow down the growth of melanoma cells.
The company presented data from one main study comparing Balimek with dacarbazine a cancer medicine used for treating melanoma. The study involved 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. The application was withdrawn after the CHMP had evaluated the documentation provided by the company and formulated lists of questions.
The company had not responded to the last round of questions at the time of the withdrawal. 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.
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.
The company informed the CHMP that there are no consequences for patients currently included in clinical trials using Balimek. If you are in a clinical trial and need more information about your treatment, contact the doctor who is giving it to you.
An assessment report is published when the application is withdrawn after the first stage of the CHMP 's evaluation is completed 'day '. Skip to main content. Veterinary regulatory Overview Research and development Marketing authorisation Post-authorisation.
Balimek: Withdrawal of the marketing authorisation application. Table of contents Overview Key facts All documents. Expand section Collapse section. List item. Key facts.
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Balimek is a medicine that contains the active substance binimetinib. It was to be available as tablets to be taken by mouth. Balimek was expected to be used for treating melanoma a type of skin cancer that had spread or could not be removed by surgery. These proteins encourage the growth of new cells. By blocking the MEK proteins, Balimek is expected to slow down the growth of melanoma cells. The company presented data from one main study comparing Balimek with dacarbazine a cancer medicine used for treating melanoma.
MEK quiz show where participants had to answer all the questions to get final prize money. Ready to Participate with questions and Answers. MEK money winning show and registration process is quite easy and anyone can participate in this money game show all you need is a good knowledge in all the fields. The registration process of MEK is very simple and any one can participate in the show.
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