Nipocalimab demonstrates positive data in pregnant patients at risk for hemolytic disease of fetus, newborn

Article

The rare condition can lead to life-threatening anemia in the fetus and currently lacks FDA-approved treatments.

According to an announcement made by the Janssen Pharmaceutical Companies of Johnson & Johnson today, phase 2 data from the open-label UNITY clinical trial of nipocalimab for the treatment of pregnant adults with high risk for severe hemolytic disease of the fetus and newborn (HDFN) offered positive topline results.

The rare condition can lead to fatal anemia in the fetus, and no therapeutics have been approved for treatment at this time. A Fast Track designation was granted by the US Food and Drug Administration (FDA) in July 2019, followed by an orphan drug status in June 2020.

"These early results represent an important step towards delivering a potential medication for expectant mothers at high risk of severe HDFN, and we are encouraged by what this treatment could mean for families affected by this potentially devastating disease," Katie Abouzahr, MD, Vice President, Autoantibody Portfolio Development Leader, Janssen Research & Development, LLC, said in a statement accompanying the news.

Results demonstrated that a majority of pregnant patients treated with nipocalimab achieved a live birth at the gestational age of 32 weeks, or after, without requiring intrauterine transfusion (IUT) at any time during pregnancy, therefore meeting the primary endpoint of the trial. Based on the safety profile observed during the approximate 20-week treatment period, further development of the monoclonal antibody is supported.

"We look forward to sharing the full phase 2 results of the UNITY trial at an upcoming scientific medical meeting while we continue to plan for a pivotal phase 3 trial," Abouzahr continued.

This article was originally published by our sister publication HCP Live.

Reference:

Janssen Reports Positive Topline Phase 2 Results for Nipocalimab in Pregnant Individuals at High Risk for Severe Hemolytic Disease of the Fetus and Newborn (HDFN). News release. Janssen Pharmaceutical Companies of Johnson & Johnson. February 06, 2023. https://www.prnewswire.com/news-releases/janssen-reports-positive-topline-phase-2-results-for-nipocalimab-in-pregnant-individuals-at-high-risk-for-severe-hemolytic-disease-of-the-fetus-and-newborn-hdfn-301738963.html

Recent Videos
Improving pediatric HPV vaccination rates: Early initiation and addressing disparities | Image Credit: blog.nemours.org.
March of Dimes 2024 Report highlights preterm birth crisis | Image Credit: marchofdimes.org
Understanding and managing postpartum hemorrhage: Insights from Kameelah Phillips, MD | Image Credit: callawomenshealth.com
Rossella Nappi, MD, discusses benefits of fezolinetant against vasomotor symptoms | Image Credit: imsociety.org
Understanding cardiovascular risk factors in women | Image Credit: cedars-sinai.org.
Updated FLUBLOK label expands influenza vaccine options for pregnant women | Image Credit: mass-vaccination-resources.org
Sheryl Kingsberg, PhD: Psychedelic RE104 for postpartum depression
JoAnn Pinkerton discusses elinzanetant's crucial role in VMS therapy | Image Credit: uvahealth.com
Elinzanetant displays positive phase 3 safety and efficacy data against VMS | Image Credit: © toeytoey - © toeytoey - stock.adobe.com.
JoAnne Pinkerton, MD, FACOG, NCMP
Related Content
© 2024 MJH Life Sciences

All rights reserved.