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Home Breaking News

Alvotech and Dr. Reddy’s collaborates for commercialization of AVT03 (denosumab) in U.S., Europe & UK

The collaboration combines Dr. Reddy’s global commercial presence with Alvotech’s proven capabilities in developing biosimilars for markets worldwide.

by NavJeevan
1 year ago
in Breaking News, Business, Companies, Health & Environment, Human Interest, Hyderabad, Joint Venture/Partnerships, National, Pharma
Reading Time: 2 mins read
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Dr. Reddy's building. PHOTO: Dr Reddy's

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NE HEALTH BUREAU
HYDERABAD/REYKJAVIK (ICELAND), MAY 21

Alvotech, a global biotech company specializing in the development and manufacture of biosimilar medicines for patients worldwide (“Alvotech”), and Dr. Reddy’s Laboratories SA, wholly-owned subsidiary of Dr. Reddy’s Laboratories Ltd., on Tuesday announced that the companies have entered into a license and supply agreement for the commercialization of AVT03, Alvotech’s biosimilar candidate to Prolia® and Xgeva® (denosumab). The collaboration combines Dr. Reddy’s global commercial presence with Alvotech’s proven capabilities in developing biosimilars for markets worldwide.

We are pleased to announce our latest strategic collaboration – with @alvotechpr for AVT03 (denosumab), a biosimilar candidate to Prolia® & Xgeva®, for patients in the United States, Europe and the United Kingdom. The collaboration combines our global commercial presence with… pic.twitter.com/sSEOb7QwqP

— Dr. Reddy’s Laboratories Ltd (@drreddys) May 21, 2024

Prolia® and Xgeva® are indicated for the treatment of various diseases including osteoporosis in postmenopausal women and prevention of skeletal-related events in adults with advanced malignancies.

  • Reddy’s gets exclusive commercialization rights in the United States (U.S.) as well as semi-exclusive rights in Europe and United Kingdom (UK)
  • Alvotech will be responsible for development and manufacture of the product

A joint press statement said that Alvotech will be responsible for development and manufacturing of the product. Dr. Reddy’s will be responsible for registration and commercialization of the product in the applicable markets. The license and supply agreement includes an upfront payment to Alvotech, with additional payments upon certain regulatory and commercialization milestones as well as sales-based payments. Dr. Reddy’s commercialization rights are exclusive for the U.S., and semi-exclusive for Europe and the UK.

Commenting on this Erez Israeli, Chief Executive Officer of Dr. Reddy’s, said “We are pleased to collaborate with Alvotech to make this denosumab biosimilar available to patients in the U.S., Europe and UK. Over the years, we have created a portfolio of biosimilar products, which are marketed in several emerging markets. Most recently, we launched bevacizumab, our first biosimilar in the UK. This strategic collaboration augments our growing portfolio of biosimilar offerings, and progresses our biosimilar journey further into the highly regulated markets. We look forward to leveraging our strong commercial capabilities in these markets to ensure patients receive access to best-in-class therapies and affordable treatment options.”

“We are proud to announce this new strategic partnership, that will enable us to increase the availability of cost-effective, critical biologic medications across multiple markets worldwide,” said Robert Wessman, Chairman and CEO of Alvotech.

He further said, “Dr. Reddy’s shares our commitment to provide better access to safe and effective biologics. Biosimilars play an increasingly important role in global healthcare systems, offering broader access to best-in-class therapies. Combining our resources will ensure that patients globally can be better served.”

Tags: AlvotechAVT03 (denosumab)biosimilar candidatecollaboratescommercializationDr. Reddy'sEuropeProliaU.S.UKXgeva
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