Eisai Commences Sales of Biogen’s Multiple Sclerosis Treatment Portfolio in India

IMT News Desk
IMT News Desk
· 3 min read
Datwyler

Eisai Pharmaceuticals India Pvt. Ltd (“Eisai India”), a leading Japanese pharmaceutical company in India, announced today that it has commenced sales of Biogen’s multiple sclerosis (MS) portfolio in India based on a collaboration agreement between Eisai India’s parent company Eisai Co., Ltd. (“Eisai”) and Biogen Inc. (“Biogen”)for India and other Asian countries.

Under the agreement, Eisai distributes and books sales for Biogen’s MS treatments,AVONEX® (interferon beta 1a), TYSABRI® (natalizumab), TECFIDERA® (dimethyl fumarate)and PLEGRIDY® (peginterferon beta-1a) in India.

The number of MS patients has increased in India in recent years. No survey has been done for MS Patients, but it is estimated that there are about ~200,000 MS patients in India. MS is being increasingly diagnosed due to an increase in the number of practicing neurologists and easy and affordable availability of magnetic resonance imaging (MRI).

“Abiding by our core philosophy of human health care and access to medicine, we strive to work in areas of unmet medical needs and make available the support needed by patients and their families for coping with the disease. MS is one such unmet disease segment and providing the patients with necessary support, we can significantly improve the quality of life of patients and give them hope to live a better life,” said Dr Sanjit Singh Lamba, Managing Director, Eisai India.

He further added, “CNS/Neuro-Psychiatry has been a therapeutic focus area for Eisai and we will continue to use our strengths in research and development. By partnering with other companies to create and bring medicines to the country, we seek to improve and enhance the quality of life of patients and their families.”

Commenting on the low awareness of MS, Saumil Mody, Vice President, Commercial Operations, Eisai India, said“ Not many people are aware about MS or understand its challenges.  Lack of awareness about the disease and its symptoms, associated social stigma, lack of skilled professionals, as well as limited access to the latest advancements in technologies among the rural population result in a majority of cases going undiagnosed. Our aim is to help address these challenges and enable patients and their families to live a better life.”

MS is an intractable disease and can only be handled by managing the symptoms, being physically active and medications that aid in delaying the progression of disease. If left untreated, patients may eventually develop severe and irreversible disabilities.

MS is an autoimmune disorder where the body’s immune system starts attacking the protective sheath covering the nerve cells in the brain and the spinal cord. MS is one of the most common neurological disorders and reason for disability in young adults. The cause of MS is yet unknown and as yet there is no cure, though there are treatments available that can help some forms of MS.

Raising awareness about MS and establishing an early diagnosis is imperative as MS is a disease that evolves over time. Eisai India has recently launched two of its in-house developed products in India – both in areas of unmet medical need. Lenvima® (Lenvatinib) indicated for radioactive iodine refractory differentiated thyroid cancer was launched in the oncologys pace in June 2017 while Fycompa® (Perampanel) indicated forpartial onset seizures was launched in the neuropsychiatry segment in August 2017.

Read Next

Glenmark Launches Winlevi® in Key European Markets for the Treatment of Acne Vulgaris
News
June 12, 2026

Glenmark Launches Winlevi® in Key European Markets for the Treatment of Acne Vulgaris

Glenmark Specialty S.A. (GSSA), a wholly owned subsidiary of Glenmark Pharmaceuticals Ltd., has announced the launch of Winlevi® (clascoterone 10 mg/g cream) across key markets in Europe. This follows the grant of marketing authorization of the product for the treatment of acne vulgaris in both adults and adolescents aged 12 to <18 years (with usage in […]
Article by: IMT News Desk
Thyrocare Expands Its Presence in Prayagraj with the Launch of Its New Diagnostic Laboratory
News
June 12, 2026

Thyrocare Expands Its Presence in Prayagraj with the Launch of Its New Diagnostic Laboratory

Thyrocare Technologies Limited has announced the set-up of its new diagnostic laboratory in Prayagraj, Uttar Pradesh, in association with SecondMedic. The new laboratory is equipped with advanced testing infrastructure and supported by trained professionals, enabling timely and error-free diagnostic results. It caters to both specialised and routine testing requirements, offering support to ongoing and preventive […]
Article by: IMT News Desk
AstraZeneca Gets CDSCO Approval for Trastuzumab Deruxtecan in HER2-Positive Breast Cancer
News
June 12, 2026

AstraZeneca Gets CDSCO Approval for Trastuzumab Deruxtecan in HER2-Positive Breast Cancer

AstraZeneca Pharma India Ltd. (AZPIL) announced that the Central Drugs Standard Control Organisation (CDSCO) has approved an additional indication for Trastuzumab Deruxtecan 100 mg/5 mL vial lyophilized powder for concentrate for solution for infusion, in combination with Pertuzumab as a first-line treatment for adult patients with unresectable or metastatic HER2-positive (IHC 3+ or ISH+) breast cancer. In India, HER2-positive breast […]
Article by: IMT News Desk
Alembic Pharmaceuticals Limited announces USFDA Tentative Approval for Larotrectinib Capsules
News
June 11, 2026

Alembic Pharmaceuticals Limited announces USFDA Tentative Approval for Larotrectinib Capsules

Alembic Pharmaceuticals Limited (Alembic) announced that it has received tentative approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Larotrectinib Capsules, 25 mg and 100 mg. The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Vitrakvi Capsules, 25 mg and 100 mg, of […]
Article by: IMT News Desk