Docetaxel Mylan
Application withdrawn
The application for this medicine has been withdrawn
docetaxel
MedicineHumanWithdrawn application
Overview
On 8 March 2010, Mylan S.A.S. officially notified the Committee for Medicinal Products for Human Use (CHMP) that it wishes to withdraw its application for a marketing authorisation for Docetaxel Mylan intended to be used to treat breast cancer, non-small-cell lung cancer, prostate cancer, gastric adenocarcinoma, and head and neck cancer.
Docetaxel Mylan is a medicine that contains the active substance docetaxel. It was to be available as a powder and solvent to be made up into a solution for infusion (drip into a vein).
Docetaxel Mylan was developed as a 'generic medicine'. This means that Docetaxel Mylan was intended to be similar to a 'reference medicine' already authorised in the European Union called Taxotere.
Docetaxel Mylan was expected to be used to treat breast cancer, non-small-cell lung cancer, prostate cancer, gastric adenocarcinoma (a type of stomach cancer) and head and neck cancer. It was to be used on its own or with other anticancer medicines.
The active substance in Docetaxel Mylan, docetaxel, belongs to the group of anticancer medicines known as the taxanes. Docetaxel blocks the ability of cells to destroy the internal 'skeleton' that allows them to divide and multiply. With the skeleton still in place, the cells cannot divide and they eventually die. Docetaxel also affects non-cancer cells such as blood cells, which can cause side effects.
The company provided data on docetaxel from the published literature. Because Docetaxel Mylan contains the same active substance as Taxotere and was to be given directly into a vein, the company did not consider additional studies on the Docetaxel Mylan to be necessary according to EU rules.
The application was withdrawn at 'day 120'. This means that the CHMP had evaluated the initial documentation provided by the company and formulated a list of questions. The company had not yet responded to the questions at the time of the withdrawal.
Based on the review of the data, at the time of the withdrawal, the CHMP had some concerns and was of the provisional opinion that Docetaxel Mylan could not have been approved.
Other substances are added to docetaxel to help it form small spherical structures called 'micelles' that are suitable for injection. However, the substances added in Docetaxel Mylan and Taxotere to form the micelles are not the same. Because of this and the complex nature of micelles themselves, the Committee had concluded that additional studies on Docetaxel Mylan were necessary, including studies on how the medicine would be treated by the body and its safety.
Therefore, at the time of the withdrawal, the CHMP was of the opinion that the company had not provided enough data to support the application for Docetaxel Mylan.
The letter from the company notifying the Agency of the withdrawal of the application is available under the tab 'All documents'.
Key facts
- Name of medicine
- Docetaxel Mylan
- Active substance
- docetaxel
- International non-proprietary name (INN) or common name
- docetaxel
- Therapeutic area (MeSH)
- Carcinoma, Non-Small-Cell Lung
- Breast Neoplasms
- Head and Neck Neoplasms
- Stomach Neoplasms
- Adenocarcinoma
- Prostatic Neoplasms
- EMA product number
- EMEA/H/C/001193
Generic
- <p>This is a generic medicine, which is developed to be the same as a medicine that has already been authorised, called the reference medicine. A generic medicine contains the same active substance(s) as the reference medicine, and is used at the same dose(s) to treat the same disease(s). For more information, see <a href="/node/69107">Generic and hybrid medicines</a>.</p>
- Marketing authorisation applicant
- Mylan S.A.S.
- Withdrawal of application
- 08/03/2010
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