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Evaxion Biotech announces Clinical Collaboration to evaluate Keytruda in melanoma patients

Latest news updates...
Oct 26

Adagene Announces the Third Clinical Trial Collaboration with Merck to Advance Anti-CD137 Agonist, ADG106

Latest Pharma Update...
Aug 23

Immutep receives FDA and IRB approval in the US for Phase IIb TACTI-003 trial in HNSCC

Immutep was granted Fast Track designation for efti to treat 1st line HNSCC patients by the US FDA in early April 2021. ...
Jul 12

M2GEN announces new collaboration with Merck to advance Cancer therapies

Another pharma collaboration for the advancement of cancer therapies ...
Mar 22

FDA Grants Priority Review to Merck’s Supplemental Biologics License Application for KEYTRUDA

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Dec 18

FDA Grants Priority Review to Merck’s Supplemental Biologics License Application for KEYTRUDA

Patients with newly diagnosed esophageal and GEJ cancer face an aggressive disease with a poor prognosis, despite the currently available treatment options...
Dec 17

KEYTRUDA Plus LENVIMA Combination Demonstrated Statistically Significant Improvement in Overall Survival

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Dec 16

Merck Receives Positive EU CHMP Opinion for KEYTRUDA as First-Line Treatment for Metastatic Microsatellite Instability

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Dec 11

I-Mab accelerates clinical development of anti-CD47 monoclonal antibody lemzoparlimab in the US and China

I-Mab's global collaboration with AbbVie will facilitate global development of lemzoparlimab...
Dec 05

KEYTRUDA plus LENVIMA met the trial’s primary endpoint of progression-free survival

LENVIMA plus everolimus were evaluated versus sunitinib for the first-line treatment of patients with advanced renal cell carcinoma...
Nov 10

BriaCell announces the overall breast cancer survival (OS) data of its lead product candidate, Bria-IMTâ„¢

Median OS of 13.3 months has been observed in the Phase I/IIa study for patients treated with Bria-IMTâ„¢ in combination with immune ...
Oct 21

Affimed and NKMax America to Study the Combination of AFM24, an EGFR-Targeted Innate Cell Engager, with SNK01 Natural Killer Cell Therapy

NKMax America has developed a proprietary NK cell expansion and activation technology platform which allows it to produce unprecedented commercial amounts of autologous and allogeneic ...
Oct 20

Merck received US FDA approval for Keytruda

FDA approves expanded indication for Merck’s KEYTRUDA (pembrolizumab) in adult patients with relapsed or refractory classical hodgkin lymphoma (cHL) ...
Oct 16

FDA Approves Expanded Indication for Merck’s KEYTRUDA in Adult Patients With classical Hodgkin Lymphoma (cHL)

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Oct 15

PharmAbcine entered into a strategic partnership with Samsung Biologic

PharmAbcine is a clinical-stage biotech company developing fully human therapeutic antibodies to treat cancer and neovascular disease...
Sep 22

Merck’s KEYTRUDA Receives Two New Approvals in Japan

Keytruda would be soon launched in Japan for the treatment of cancerous tumors...
Aug 27

PharmAbcine signs manufacturing agreement with Binex

PharmAbcine signs long-term contract manufacturing organization agreement for Olinvacimab with Binex ...
Jun 27

Scientists Create Antibody That Defeats Coronavirus in Lab

The experimental antibody has neutralized the virus in cell cultures. While that's early in the drug development process, the antibody may help prevent or ...
May 05

US drug market will see Novartis, Merck and Allergan to hike their prices on entire product portfolio

Novartis,Allergan and Merck joins the list after Pfizer,increases drug prices in US...
Jan 07

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