Amgen Delivers Mixed Data For Rocatinlimab In Atopic Dermatitis, Uplizna In Myasthenia Gravis

Four Of Seven More AD Trials To Read Out Over Next Year

Rocatinlimab met its Phase III endpoints with results that appear uncompetitive with AD market leader Dupixent, while Uplizna may offer a compelling twice-yearly gMG treatment option.

Long Exposure Night Time Rocket Launch - Planet Earth with a spectacular sunset
HORIZON is the first of eight ROCKET studies in atopic dermatitis • Source: Shutterstock

Amgen, Inc. made an unusual move to release topline Phase III results for its Kyowa Kirin Co., Ltd.-partnered OX40 inhibitor rocatinlimab in atopic dermatitis (AD) and its CD19 inhibitor Uplizna (inebilizumab) in generalized myasthenia gravis (gMG), holding an analyst call after the stock market closed on 24 September and forgoing press releases. The clinical trials for both drugs delivered statistically significant results, but while most analysts saw a role for Uplizna in gMG, all questioned rocatinlimab’s ability to compete in AD.

Key Takeaways
  • Amgen reported the first Phase III results for OX40 inhibitor rocatinlimab in atopic dermatitis and CD19 inhibitor Uplizna (inebilizumab) in generalized myasthenia gravis, which generated mixed reactions.

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Clinical Trials

Lilly’s Orforglipron Makes Strong Showing In Diabetic Obesity Population

 

The drugmaker announced topline results from the Phase III ATTAIN-2 trial in overweight/obese patients with type 2 diabetes and plans to file for approval.

Regeneron Plans To File Cemdisiran For gMG But Will Face Tough Market

 

Head of hematology clinical development Andres Sirulnik talked to Scrip about the positive Phase III results for the siRNA medicine.

Pipeline Watch: Twelve Approvals And Two Phase III Readouts

Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.

Argenx’s Vyvgart Positioned For Broadest Label In Myasthenia Gravis

 

The company reported positive Phase III data in individuals with gMG who are ACHr-Ab seronegative, providing an expansion opportunity.

More from R&D

Pipeline Watch: Twelve Approvals And Two Phase III Readouts

Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.

Argenx’s Vyvgart Positioned For Broadest Label In Myasthenia Gravis

 

The company reported positive Phase III data in individuals with gMG who are ACHr-Ab seronegative, providing an expansion opportunity.

Pipeline-In-A-Product: A Retrospective On The Development Of Dupixent

 

Dupixent’s success across eight indications is a model other drugmakers would like to replicate. R&D leaders at Sanofi and Regeneron reflect back on the development strategy that built the $15bn product.