MedPath

FDA Approves Roche's Injectable Ocrevus, Novartis' Kisqali, and Lilly's Ebglyss; WHO Clears Bavarian Nordic’s Mpox Vaccine

• Roche's Ocrevus gains FDA approval for an injectable version, offering a new administration option for multiple sclerosis patients. • Novartis' Kisqali receives FDA approval to reduce the risk of recurrence in HR+/HER2- early breast cancer, expanding treatment options. • Lilly's Ebglyss (lebrikizumab-lbkz) is approved for moderate-to-severe atopic dermatitis in adults and children 12 years and older. • The World Health Organization clears Bavarian Nordic’s mpox vaccine, marking the first WHO-approved shot for mpox containment.

The FDA has recently approved several new treatments, offering advancements in the management of multiple sclerosis, breast cancer, and atopic dermatitis. Simultaneously, the World Health Organization (WHO) has cleared a crucial vaccine for mpox, marking a significant step in global health efforts.

Roche's Ocrevus Receives Approval for Injectable Formulation

Roche's Ocrevus, a well-established therapy for multiple sclerosis, has now been approved by the FDA in an injectable form. This new formulation offers an alternative administration route for patients, potentially improving convenience and adherence. Ocrevus has demonstrated efficacy in reducing disease activity and slowing disability progression in relapsing and progressive forms of MS.

Novartis' Kisqali Approved to Reduce Breast Cancer Recurrence

Novartis has secured FDA approval for Kisqali to reduce the risk of recurrence in individuals with HR+/HER2- early breast cancer. This approval marks a significant advancement in adjuvant therapy, providing a new option for patients at risk of cancer recurrence. Kisqali, in combination with endocrine therapy, has shown a statistically significant improvement in disease-free survival, offering hope for improved long-term outcomes.

Lilly's Ebglyss (lebrikizumab-lbkz) Approved for Atopic Dermatitis

Lilly's Ebglyss (lebrikizumab-lbkz) has gained FDA approval for the treatment of moderate-to-severe atopic dermatitis in adults and children 12 years and older. This approval provides a new biologic option for patients who have not responded adequately to topical therapies. Lebrikizumab, a monoclonal antibody targeting IL-13, has demonstrated significant improvements in skin clearance and itch reduction in clinical trials.

WHO Approves Bavarian Nordic’s Mpox Vaccine

The World Health Organization (WHO) has cleared Bavarian Nordic’s mpox vaccine, the first such shot to be approved by the agency for containing the spread of the disease in badly hit African countries. This approval is a critical step in controlling the mpox outbreak, particularly in regions where the disease is endemic. The vaccine has shown promising results in preventing mpox infection and reducing the severity of symptoms.

Other Industry Updates

In other industry news, MaxCyte announced a partnership with Kamau Therapeutics, while Revance Therapeutics reported that Crown Laboratories failed to initiate a tender offer by the deadline, impacting their acquisition agreement. Additionally, Cigna’s pharmacy benefit manager Express Scripts has sued the Federal Trade Commission, demanding a retraction of a recent report critical of drug spending negotiation practices. Nura Bio raised $68 million in funding, and Arzeda closed an oversubscribed $38 million funding round.
Subscribe Icon

Stay Updated with Our Daily Newsletter

Get the latest pharmaceutical insights, research highlights, and industry updates delivered to your inbox every day.

Related Topics

Reference News

[1]
Rx Rundown: MaxCyte, Roche, and more - Medical Marketing and Media
mmm-online.com · Sep 20, 2024

MaxCyte partners with Kamau Therapeutics, Arvato Systems with Advanco, Revance Therapeutics' acquisition impacted by Cro...

© Copyright 2025. All Rights Reserved by MedPath