


Reminder: The outer packaging is for reference only, please purchase and use under the guidance of a pharmacist. For read by medical and pharmaceutical professionals only.
Trabectedin for Injection is a chemotherapeutic agent that has received tentative approval from the U.S. FDA under section 505(b)(2) of the Federal Food, Drug, and Cosmetic Act (FD&C Act). This drug is primarily administered via intravenous injection, and it is designed to work by interfering with the DNA of cancer cells, thereby inhibiting their ability to divide and grow. The mechanism of action of Trabectedin involves DNA minor groove binding and intercalation, leading to the disruption of DNA transcription and repair, which ultimately induces cell death, particularly in neoplastic tissues.
Although the drug has achieved tentative approval, it is not yet authorized for marketing until the expiration of relevant patent protections and resolution of any ongoing legal issues related to patent infringement claims. This status means that the drug cannot be legally marketed, and its labeling cannot be used for public distribution until the FDA issues its final approval. The final approval will depend on further court proceedings related to patent disputes and the resolution of exclusivity protections.
Trabectedin for Injection is indicated for use in the treatment of soft tissue sarcoma and ovarian cancer. It is typically employed for patients whose cancer has either relapsed or is resistant to standard chemotherapy treatments. Specific details regarding the exact therapeutic use in the indicated population will be available upon final FDA approval. Not specified in the specification.
The recommended dose is 1.5 mg/m², administered via central venous infusion once every 21 days, with each infusion lasting 24 hours, until disease progression or unacceptable toxicity occurs.
