Category Research

Epcoritamab Combination Therapy Shows High Response Rates in R/R Follicular Lymphoma Trial

Genmab has announced promising results from the Phase 1b/2 EPCORE® NHL-2 trial, which evaluated a fixed-duration regimen of epcoritamab, a T-cell engaging bispecific antibody, in combination with lenalidomide and rituximab (R2) in adult patients with relapsed or refractory (R/R) follicular…

Read MoreEpcoritamab Combination Therapy Shows High Response Rates in R/R Follicular Lymphoma Trial

Epcoritamab Monotherapy Shows High Response Rates in R/R CLL Trial

Genmab has announced promising results from the Phase 1b/2 EPCORE® CLL-1 clinical trial evaluating epcoritamab, a T-cell engaging bispecific antibody, in patients with relapsed or refractory chronic lymphocytic leukemia (R/R CLL). Epcoritamab, administered subcutaneously as monotherapy, demonstrated an overall response…

Read MoreEpcoritamab Monotherapy Shows High Response Rates in R/R CLL Trial

Stoke Therapeutics Presents Data Supporting Zorevunersen as Treatment for Dravet Syndrome

Stoke Therapeutics has announced new data from its Phase 1/2a and open-label extension (OLE) studies on zorevunersen, a potential disease-modifying treatment for Dravet syndrome. The data revealed significant and lasting reductions in convulsive seizure frequency in patients who received zorevunersen…

Read MoreStoke Therapeutics Presents Data Supporting Zorevunersen as Treatment for Dravet Syndrome

Alithea Genomics Unveils Full-Length DRUG-Seq to Enhance Transcriptomics in Drug Discovery

Alithea Genomics, a leading innovator in large-scale RNA sequencing and transcriptomics, has unveiled its latest technological advancement: the MERCURIUS™ Full-Length DRUG-seq library preparation platform. This new solution represents a groundbreaking approach in RNA sequencing, combining massive sample multiplexing, an extraction-free…

Read MoreAlithea Genomics Unveils Full-Length DRUG-Seq to Enhance Transcriptomics in Drug Discovery

Intra-Cellular Therapies Files sNDA for CAPLYTA® as Adjunctive MDD Treatment

Intra-Cellular Therapies, Inc. (Nasdaq: ITCI), a biopharmaceutical company dedicated to central nervous system (CNS) therapeutics, has announced the submission of a supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration (FDA). The application seeks approval for CAPLYTA…

Read MoreIntra-Cellular Therapies Files sNDA for CAPLYTA® as Adjunctive MDD Treatment