DLBCL
![Roche reveals blood cancer plans post-COVID](https://pharmtales.com/wp-content/uploads/2023/10/Roche-unveils-its-blood-cancer-strategy-after-COVID-19-boost.jpg)
Roche unveils its blood cancer strategy after COVID-19 boost
While Roche has seen a decline in COVID-19 drug sales after the pandemic boom, the company is experiencing a resurgence ...
![2023's Drug Approvals, Oncology Approvals, bispecific antibody approvals, approvals, DLBCL, multiple myeloma, Non-Oncology, Drug Approval, FDA Approvals 2023,](https://pharmtales.com/wp-content/uploads/2023/08/FDA-criticizes-Intas-and-Ipca-for-manufacturing-flaws-at-three-Indian-factories.jpg)
Unveiling 2023’s Drug Approvals: Beyond Oncology Boundaries
In the ever-evolving realm of oncology of 2023 emerges as a pivotal era characterized by a wave of significant approvals ...
![AbbVie’s Epcoritamab Gets CHMP Nod for DLBCL](https://pharmtales.com/wp-content/uploads/2023/07/AbbVies-Epcoritamab-EPKINLY-Receives-Positive-CHMP-Opinion-for-DLBCL-Treatment.jpg)
AbbVie’s Epcoritamab (EPKINLY) Receives Positive CHMP Opinion for DLBCL Treatment
Source – AbbVieAbbVie and Genmab’s potential blockbuster drug epcoritamab has received a favorable recommendation for conditional approval in the EU ...
![ADC Therapeutics Halts LOTIS-9 Trial of Zynlonta for DLBCL Patients](https://pharmtales.com/wp-content/uploads/2023/07/Discontinuation-of-LOTIS-9-Trial_-Zynlonta-in-Unfit-DLBCL-Patients.jpg)
Discontinuation of LOTIS-9 Trial: Zynlonta in Unfit DLBCL Patients
Source – ADC Therapeutics On July 20, 2023, ADC Therapeutics announced its decision to discontinue the Phase II LOTIS-9 clinical ...
![After 7 patient fatalities and 5 other serious adverse events, ADC suspends the Zynlonta research](https://pharmtales.com/wp-content/uploads/2023/07/After-7-patient-fatalities-and-5-other-serious-adverse-events-ADC-suspends-the-Zynlonta-research.jpg)
After 7 patient fatalities and 5 other serious adverse events, ADC suspends the Zynlonta research
Source – ADC Therapeutics ADC Therapeutics has halted enrollment in a Phase II combination trial for Zynlonta following the investigation ...
![Roche's Columvi (glofitamab) for patients with R_R diffuse large B-cell lymphoma has received approval from the European Commission](https://pharmtales.com/wp-content/uploads/2023/07/Roches-Columvi-glofitamab-for-patients-with-R_R-diffuse-large-B-cell-lymphoma-has-received-approval-from-the-European-Commission.jpg)
Roche’s Columvi (glofitamab) for patients with R/R diffuse large B-cell lymphoma has received approval from the European Commission
Source – Roche On 11 July 2023 Roche announced that the European Commission (EC) has given conditional approval for Columvi ...
![Roche's Columvi and AbbVie's Epkinly: The Battle for Breakthroughs in Large B-Cell Lymphoma Treatment](https://pharmtales.com/wp-content/uploads/2023/06/Roches-Columvi-and-AbbVies-Epkinly_-The-Battle-for-Breakthroughs-in-Large-B-Cell-Lymphoma-Treatment.jpg)
Roche’s Columvi and AbbVie’s Epkinly: The Battle for Breakthroughs in Large b Cell Lymphoma Treatment
Roche’s Columvi (glofitamab) receives FDA accelerated approval for treatment of Large b Cell Lymphoma, sparking a rivalry with AbbVie and ...
![Glofitamab-gxbm receives FDA approval for relapsing or resistant DLBCL](https://pharmtales.com/wp-content/uploads/2023/06/Glofitamab-gxbm-receives-FDA-approval-for-relapsing-or-resistant-DLBCL.jpg)
Glofitamab-gxbm receives FDA approval for relapsing or resistant DLBCL
Source – Roche Columvi (Glofitamab-gxbm) has been given expedited clearance by the FDA for the treatment of adult patients with ...
![Epkinly: First And Only Fda-Approved Bispecific Antibody For Relapsed Or Refractory Diffuse Large B-Cell Lymphoma (Dlbcl)](https://pharmtales.com/wp-content/uploads/2023/06/Epkinly-First-And-Only-Fda-Approved-Bispecific-Antibody-For-Relapsed-Or-Refractory-Diffuse-Large-B-Cell-Lymphoma-Dlbcl-1.jpg)
Epkinly: FDA-Approved Bispecific Antibody for DLBCL
On May 19, 2023, AbbVie announced that the U.S. Food and Drug Administration (FDA) granted approval to EPKINLYTM (epcoritamab-bysp) as ...
![](https://pharmtales.com/wp-content/uploads/2023/06/EPCORITAMAB-RECEIVES-FDA-APPROVAL-FOR-RELAPSEDREFRACTORY-DLBCL.jpg)
EPCORITAMAB RECEIVES FDA APPROVAL FOR RELAPSED/REFRACTORY DLBCL
The FDA has granted approval to epcoritamab-bysp (Epkinly), the first T-cell–engaging bispecific antibody, for the treatment of relapsed/refractory diffuse large ...