Venus Remedies gets UK marketing authorization for bleomycin 15,000 IU

Venus Remedies has bagged the market authorization in the United Kingdom for bleomycin 15,000 IU powder for solution for injection/infusion by its German subsidiary, Venus Pharma GmbH. This milestone, according to the company not only expands the pharma giant's global presence but also underscores its commitment to advancing cancer care with innovative solutions.

Bleomycin 15,000 IU is a potent medication that contains the active ingredient bleomycin sulfate. It belongs to a group of medicines known as cytostatic drugs, specifically designed to combat cancer. This class of medications, often referred to as chemotherapy, is renowned for its effectiveness in targeting cancer cells and preventing their uncontrolled division.

Its versatile applications include the treatment of certain types of squamous cell carcinomas in the head and neck, cervix, and external genitalia. It also serves as a panacea in treating severe types of lymph node cancers, such as Hodgkin's disease and non-Hodgkin's lymphoma of intermediate and high malignancy, testicular cancer, and fluid accumulation in the lungs, often associated with cancer.

Bleomycin can be administered as a standalone treatment or in combination with other cancer medications and radiotherapy. Its effectiveness and utility in cancer treatment have earned it market authorizations in numerous countries worldwide.

Venus Remedies holds a total of 15 market authorizations for bleomycin products across the globe. As part of its efforts to make bleomycin more accessible, the company has submitted sixteen additional applications to Ministries of Health (MOHs) around the world. Venus has secured 15 registrations for this drug across various regions, including Africa, Asia, the Middle East, the Commonwealth of Independent States (CIS), North America, and South America.

"Our mission is to improve the lives of cancer patients by providing cutting-edge treatments. The UK's market authorization for bleomycin 15,000 IU powder for solution for injection/infusion is a significant step towards realizing this mission. We remain dedicated to enhancing healthcare solutions and are committed to pursuing additional authorizations to reach even more patients in need," stated Saransh Chaudhary, CEO, Venus Medicine Research Center (VMRC).

For Venus Pharma GmbH, the achievement of receiving market authorization from a regulatory agency like the Medicines and Healthcare products Regulatory Agency (MHRA) in the United Kingdom is a significant validation of the company's commitment to pharmaceutical excellence.

Ashutosh Jain, CEO, Venus Pharma GmbH, stated that that obtaining market authorization from MHRA is a momentous accomplishment for Venus Pharma GmbH. It enables the company to play a pivotal role in advancing cancer care and improving the quality of life for patients facing this challenging disease.

Optimize Your trial insights with Clival Database.

Are you exhausted from the uncertainty of trial insights pricing? Clival Database ensures the clarity in the midst of the global scenario for clinical trials to you.

Clival Database is one of the best databases that offers an outstanding number of clinical trial data in terms of 50,000+ molecules and from primary regulatory markets as well as new entrants like Indian and Chinese markets.

With Clival, you get accurate positioning of historical sales data, patent database, company profiling, safety & efficacy, and prediction of launch of new innovative molecules helping you to align your research and driving down the cost.

To add value, we further break down our analytics for you so that improving your operational effectiveness; optimizing your clinical trials; and offering you accurate and high-quality data at lowest possible prices becomes possible.

Elevate your trial success rate with the cutting-edge insights from Clival database.

Check it out today and make more informed sourcing decisions! Learn More!