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FDA Grants Priority Review to Epcoritamab-bysp for Relapsed or Refractory Follicular Lymphoma

If approved, epcoritamab (DuoBody CD3xCD20; AbbVie, Genmab) would be the first and only subcutaneous bispecific antibody for treatment in this patient population.

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U.S. Food and Drug Administration (FDA) Grants Priority Review of Epcoritamab (EPKINLY®) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma (FL)

/PRNewswire/ -- AbbVie (NYSE: ABBV) today announced that the U.S. Food and Drug Administration (FDA) has granted Priority Review of the supplemental Biologics...

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New Data for Bispecific Antibody Epcoritamab (DuoBody® CD3xCD20) Shows Strong, Durable Treatment Response for Patients with Difficult-To-Treat Relapsed/Refractory (R/R) Follicular Lymphoma (FL)

New Data for Bispecific Antibody Epcoritamab (DuoBody® CD3xCD20) Shows Strong, Durable Treatment Response for Patients with Difficult-To-Treat Relapsed/Refractory (R/R) Follicular Lymphoma (FL)
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New Data For Bispecific Antibody Epcoritamab (Duobody® Cd3xcd20) Shows Strong, Durable Treatment Response For Patients With Difficult-To-Treat Relapse...

New Data For Bispecific Antibody Epcoritamab (Duobody® Cd3xcd20) Shows Strong, Durable Treatment Response For Patients With Difficult-To-Treat Relapse...
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New Data for Bispecific Antibody Epcoritamab (DuoBody® CD3xCD20) Shows Strong, Durable Treatment Response for Patients with Difficult-To-Treat Relapsed/Refractory (R/R) Follicular Lymphoma (FL)

/PRNewswire/ -- AbbVie (NYSE: ABBV) and Genmab A/S (Nasdaq: GMAB) announced today that adult patients with relapsed/refractory (R/R) follicular lymphoma (FL)...

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FDA to Speed Up Epkinly Development for Relapsed/Refractory Follicular Lymphoma

The Food and Drug Administration granted a Breakthrough Therapy Designation to Epkinly to treat patients with relapsed or refractory follicular lymphoma.

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AbbVie's lymphoma drug Epkinly gets green light from FDA, EU

AbbVie's lymphoma drug Epkinly gets green light from FDA, EU
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EMA Validates Application for Epcoritamab in Relapsed/Refractory Follicular Lymphoma

The European Medicines Agency has validated a type II application for the investigational T-cell engaging bispecific antibody epcoritamab-bysp for patients with relapsed/refractory follicular lymphoma following at least 2 prior lines of therapy

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FDA Grants Breakthrough Therapy Designation to Epcoritamab for Follicular Lymphoma

The update followed results from the phase 1/2 EPCORE NHL-1 clinical trial evaluating the safety and preliminary efficacy of the drug, including in individuals with relapsed or refractory follicular lymphoma.

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Abbvie Announces U.S. Food And Drug Administration (FDA) And European Medicines Agency (EMA) Updates For Epcoritamab (EPKINLY®/TEPKINLY®) For The Trea...

Abbvie Announces U.S. Food And Drug Administration (FDA) And European Medicines Agency (EMA) Updates For Epcoritamab (EPKINLY®/TEPKINLY®) For The Trea...
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