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Zumutor Biologics Advances Cancer Care with Novel Immunotherapy ZM008: A First-in-Class Anti LLT1 Antibody

As the ZM008-001 clinical trial progresses, the medical community eagerly awaits the results, which could lead the way for a new era in cancer ...
Jun 13

Nasal Immunotherapy Shows Promise in Reducing Inflammation and Boosting Cognitive Function in Alzheimer's Disease

The discovery of nasal immunotherapy with anti-CD3 as a potential treatment for Alzheimer's disease represents a ray of hope for the millions of ...
Sep 15

Is Omicron Dangerous? Know the real truth

In fact, regarding the Omicron variant, doctors believe that the Omicron variant is more dangerous than the Delta variant of the corona. However, it is ...
Jan 11

WuXi Biologics launches a new GMP commercial drug product facility

Latest Pharma news updates...
Nov 02

Agomab Therapeutics to acquire Origo Biopharma

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Oct 29

Atreca and Bill & Melinda Gates Medical Research Institute to develop a Monoclonal Antibody to cure Malaria

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Oct 23

Enzolytics Inc. and Samsung Biologics joins hands for Anti-HIV and Anti-SARS-CoV-2 Monoclonal Antibody Therapies

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Oct 12

Boehringer Ingelheim and Invetx collaborates to advance monoclonal antibody biotherapeutics in animal health

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Sep 29

WHO recommends antibody treatment for covid patients at high risk of hospital admission

And for severely ill patients who have no natural antibodies to covid-19 ...
Sep 27

Tonix Pharmaceutical to develop precision medicine techniques for COVID-19 Vaccines and Therapeutics

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Sep 27

Precision BioSciences and Tiziana Life Sciences announce exclusive license agreement to evaluate Foralumab

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Sep 06

ImmixBio and BeiGene to evaluate combination of IMX-110 and Tislelizumab in solid tumors

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Aug 31

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

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Aug 23

GSK and Vir Biotechnology announce joint procurement agreement with European Commission for COVID-19 treatment, Sotrovimab

Latest pharma news update...
Aug 02

FDA Clearance of IND for FPI-1966, Radiopharmaceutical for Head and Neck and Bladder Cancers Expressing FGFR3

Fusion Pharmaceuticals Announces FDA Clearance of IND for FPI-1966 ...
Jul 30

FDA Clearance of IND for FPI-1966, Radiopharmaceutical for Head and Neck and Bladder Cancers Expressing FGFR3

Fusion Pharmaceuticals Announces FDA Clearance of IND for FPI-1966 ...
Jul 30

ViiV Healthcare and Halozyme enter global collaboration and license agreement for ENHANZE drug delivery technology

Halozyme’s drug delivery technology provides the opportunity to administer large volume subcutaneous injections that may enable dosing intervals of every three months and up ...
Jun 22

GSK and iTeos Therapeutics announce development and commercialisation collaboration for EOS-448

With this collaboration GSK is uniquely positioned with access to antibodies that synergistically target all three known CD226 checkpoints - TIGIT, CD96 and PVRIG....
Jun 14

FDA authorizes monoclonal antibody therapy for emergency use in some patients 12 and older

The authorization is specifically for those with mild-to-moderate Covid-19, who are at risk of getting much sicker...
May 27

GSK and Vir Biotechnology starts EMA rolling review of VIR-7831 (sotrovimab) for treatment of COVID-19

GSK's Covid product could be soon in the market after the emergency medical application review...
May 11

Sorrento receives FDA clearance Phase 2 study for Sti-3031 ; Advanced Urothelial Carcinoma

Sorrento intends to combine a variety of its proprietary mAbs in conjunction with the ADNAB technology platform...
Apr 28

Samsung Biologics and TG Therapeutics expand collaboration for the large scale manufacture of Ublituximab

Pharma Update ; Samsung expands capacity ; Ublituximab ...
Apr 26

Exelixis ; U.S. FDA accepts investigational new drug application for XB002 in patients with Advanced Solid Tumors

New drug for treating advanced tumour under investigation...
Apr 07

GSK and Vir Biotechnology requests emergency use authorization to FDA for VIR-7831 for treatment of COVID-19

The FDA EUA submission is based on an interim analysis of efficacy and safety data from the Phase 3 COMET-ICE ...
Mar 27

GSK and Vir Biotechnology requests emergency use authorization to FDA for VIR-7831 for treatment of COVID-19

The FDA EUA submission is based on an interim analysis of efficacy and safety data from the Phase 3 COMET-ICE ...
Mar 27

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