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Biological Treatment Articles & Analysis

8 news found

What do we do with the wastewater generated by the pharmaceutical industry?

What do we do with the wastewater generated by the pharmaceutical industry?

When the wastewater generated by the pharmaceutical industries has a high organic matter content, Salher’s biological treatment with a moving bed (MBBR) is the most suitable. The particularity of this wastewater is that its micropollutants are resistant to conventional treatments, so in some cases it is necessary to include in the basic ...

BySalher


BRIM Biotechnology receives FDA Orphan Drug Designation for BRM424 to treat neurotrophic keratitis

BRIM Biotechnology receives FDA Orphan Drug Designation for BRM424 to treat neurotrophic keratitis

Haishan Jang, Chairwoman and CEO of BRIM Biotechnology, commented, “Receiving FDA orphan drug designation allows us to proceed confidently with plans to advance the development of BRM424, a novel, first-in-class, potential treatment for NK. Clinically, the treatment of NK is very complicated, and there is a lack of effective and affordable ...

ByBRIM Biotechnology, Inc.


First Completion of a Full Treatment Workflow in the First European Hospital-Based BNCT Facility

First Completion of a Full Treatment Workflow in the First European Hospital-Based BNCT Facility

BNCT has the potential to deliver highly effective, cell-localized radiation therapy to treat tumors with minimal impact on the patient's quality of life compared to other available treatment options, such as radiation, chemotherapy or biological treatment modalities. ...

ByNeutron Therapeutics, Inc.


BriaCell Secures License for a Promising Novel Anti-Cancer Agent

BriaCell Secures License for a Promising Novel Anti-Cancer Agent

(Nasdaq: BCTX, BCTXW) (TSX: BCT) (“BriaCell” or the “Company”) , a clinical-stage biotechnology company specializing in targeted immunotherapies for cancer, announces that it has secured an exclusive license from University of Maryland, Baltimore County (UMBC) to develop and commercialize Soluble CD80 (sCD80) as a biologic agent for the ...

ByBriaCell Therapeutics Corp.


First Simulated Patient Treatment Carried Out in the First Hospital-Based BNCT Facility in Europe

First Simulated Patient Treatment Carried Out in the First Hospital-Based BNCT Facility in Europe

BNCT has the potential to deliver highly effective and cell-localized radiation therapy to treat tumors with minimal impact on the patient’s quality of life compared to other radiation, chemotherapy or biological treatment modalities currently in use. Neutron Therapeutics Inc. and the Helsinki University Hospital are collaborating to launch the first ...

ByNeutron Therapeutics, Inc.


Aclys Bio and Genmab Enter Research and Commercial License Option Agreement

Aclys Bio and Genmab Enter Research and Commercial License Option Agreement

January 26, 2022 – Aclys Bio Corp (“Aclys”), a company discovering and developing precision biologics for the treatment of cancer, earlier this month announced a new exclusive research and commercial license option agreement with Genmab A/S (Nasdaq: GMAB), an international biotech company specializing in the creation and development of ...

ByCeldara Medical, LLC


Accelerating Lupus Drug Discovery & Development - Fireside Chat with Experts in SLE Research

Accelerating Lupus Drug Discovery & Development - Fireside Chat with Experts in SLE Research

Genuity Science is bringing together a distinguished panel of experts from academia, research and industry to discuss opportunities and advancements in developing better treatments for systemic lupus erythematosus (SLE). SLE is a chronic and relapsing autoimmune disease characterized by a break-down of self-tolerance that leads to tissue inflammation and multiorgan damage. SLE ...

ByGenuity Science


Lilly`s Mirikizumab Helps Patients Achieve Clinical Remission and Improves Symptoms in Adults with Ulcerative Colitis in 12-Week Phase 3 Induction Study

Lilly`s Mirikizumab Helps Patients Achieve Clinical Remission and Improves Symptoms in Adults with Ulcerative Colitis in 12-Week Phase 3 Induction Study

"Results of this study provide further clinical evidence of the potential for mirikizumab to become the first anti-IL-23p19 biologic for the treatment of ulcerative colitis." In LUCENT-1, mirikizumab met the primary endpoint of clinical remission at Week 12 compared to placebo (p Mirikizumab also achieved all key secondary endpoints compared to placebo at Week ...

ByEli Lilly and Company

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