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Drug Interaction Articles & Analysis

26 news found

CD Formulation Offers Robust Expertise in Pharmacology to Aid Veterinary Drug Development

CD Formulation Offers Robust Expertise in Pharmacology to Aid Veterinary Drug Development

A critical aspect of drug development is understanding the interaction between drugs and biological systems, particularly for veterinary applications where species-specific responses can vary substantially. ...

ByCD Formulation


Alfa Chemistry: Custom Design Takes Organs-On-Chips to the Next Level

Alfa Chemistry: Custom Design Takes Organs-On-Chips to the Next Level

This cutting-edge technology provides scientists and researchers with an innovative platform to study human organs in a way that was previously impossible, promising to accelerate drug discovery, reduce the need for animal testing and ultimately transform the future of medicine. ...

ByAlfa Chemistry


CD ComputaBio Boosts Small Molecule Drug Development with Protein-Small Molecule Docking Service

CD ComputaBio Boosts Small Molecule Drug Development with Protein-Small Molecule Docking Service

It plays a crucial role in drug design and screening, as it enables modeling and prediction of interactions between proteins and small molecules, allowing customers to better understand drug mechanisms of action and optimize candidate compounds. CD ComputaBio’s Protein-Small Molecule Docking service utilizes state-of-the-art computational ...

ByCD ComputaBio


The Importance of Optimal Medical Therapy (OMT) and Collaborative Care

The Importance of Optimal Medical Therapy (OMT) and Collaborative Care

The HFSA Optimal Medical Therapy in Heart Failure (OMT-HF) program can help your patients achieve their best outcomes. An estimated 6.5 million Americans have heart failure (HF). This year alone another 960,000 will likely be diagnosed with this condition. Chances are several of your patients are in this group. Are they receiving the optimal medical therapy (OMT), that helps them achieve ...

ByHeart Failure Society of America, Inc. (HFSA)


Cellworks Expands into Precision Pharma to Accelerate the Development of Cancer Drugs and Revive Shelved Pharmaceutical Assets

Cellworks Expands into Precision Pharma to Accelerate the Development of Cancer Drugs and Revive Shelved Pharmaceutical Assets

The Cellworks platform uses computational biosimulation to model signaling pathways, master regulators, hallmark behaviors of cancer, and drug interactions with each patient’s unique disease network. Biosimulation stratifies treatment options according therapeutic impact and enables precision clinical trials that promises to transform the ...

ByCellworks Research India Private Limited


CD BioGlyco Released Characterization Service of Glycosylation in Protein Drugs

CD BioGlyco Released Characterization Service of Glycosylation in Protein Drugs

Although the drugs themselves are complicated, it is urgent to develop techniques to characterize glycosylation in order to better evaluate their effects. One of the most significant post-translational modifications during protein characterization is glycosylation. It affects the drug's biological activity, serum half-life, stability, and immunogenicity, which ...

ByCD BioGlyco.


Leveraging protein DNA/RNA interactions in drug discovery

Leveraging protein DNA/RNA interactions in drug discovery

The field of protein DNA/RNA interactions is an expanding area of research. These interactions affect fundamental processes and as a result, relevant protein DNA/RNA processing complexes and their associated mechanisms provide interesting therapeutic targets to researchers. ...

ByCresset Group


FDA Approves Taiho’s LYTGOBI® (futibatinib) Tablets for Previously Treated, Unresectable, Locally Advanced or Metastatic Intrahepatic Cholangiocarcinoma

FDA Approves Taiho’s LYTGOBI® (futibatinib) Tablets for Previously Treated, Unresectable, Locally Advanced or Metastatic Intrahepatic Cholangiocarcinoma

LYTGOBI previously received breakthrough, orphan drug and priority review designations from the FDA. PRINCETON, N.J., September 30, 2022 – Taiho Oncology, Inc. and Taiho Pharmaceutical Co., Ltd. announced today that the U.S. Food and Drug Administration (FDA) has approved LYTGOBI® tablets for the treatment of adult patients with previously treated, ...

ByTaiho Oncology, Inc.


CD Formulation Is Able to Conduct API-Excipient Compatibility Analysis for Drug Development

CD Formulation Is Able to Conduct API-Excipient Compatibility Analysis for Drug Development

We know that a drug substance is usually more stable by itself than in a formulation with excipients. Inappropriate dosage forms can interact with drug substances and in worst cases can even cause drug degradation,” says the Marketing Chief of CD Formulation. ...

ByCD Formulation


Amgen And Lance Bass Partner To Encourage People To Do A `Double Take` To Recognize The Early Signs Of Psoriatic Arthritis

Amgen And Lance Bass Partner To Encourage People To Do A `Double Take` To Recognize The Early Signs Of Psoriatic Arthritis

THOUSAND OAKS, Calif., May 12, 2022 /PRNewswire/ -- Amgen (NASDAQ:AMGN) and Otezla® (apremilast) have partnered with pop icon and entrepreneur Lance Bass, for the Double Take campaign to empower people to take action when it comes to psoriatic arthritis. As a singer, dancer and entertainer, Bass understands the importance of staying in tune with your body. Through the campaign, he has created ...

ByAmgen Inc.


BioXcel Therapeutics Announces FDA Approval of IGALMI (dexmedetomidine) Sublingual Film for Acute Treatment of Agitation Associated with Schizophrenia or Bipolar I or II Disorder in Adults

BioXcel Therapeutics Announces FDA Approval of IGALMI (dexmedetomidine) Sublingual Film for Acute Treatment of Agitation Associated with Schizophrenia or Bipolar I or II Disorder in Adults

“With this landmark achievement of our first approved drug, we have taken a monumental step toward our mission of bringing transformative medicines in neuroscience to patients using our AI platform. ...

ByBioXcel Therapeutics, Inc.


Gain Therapeutics Presents Preclinical Data On Its Structurally Targeted Allosteric Regulators In GBA1 Gaucher Disease At The WORLDSymposium 2022

Gain Therapeutics Presents Preclinical Data On Its Structurally Targeted Allosteric Regulators In GBA1 Gaucher Disease At The WORLDSymposium 2022

(Nasdaq: GANX) (“Gain”), a biotechnology company transforming the drug discovery paradigm with structurally targeted allosteric regulators (STARs) identified with its proprietary computational discovery platform, today presented new pre-clinical data from its Gaucher Disease (GD) program. ...

ByGain Therapeutics, Inc.


Gain Therapeutics Outlines Key Objectives For 2022 Following Its Inaugural R&D Day

Gain Therapeutics Outlines Key Objectives For 2022 Following Its Inaugural R&D Day

” Gain Therapeutics is leading the wave of innovation in the field of allosteric drug discovery and is one of the pioneers in the field of computational biology. ...

ByGain Therapeutics, Inc.


Gain Therapeutics Announces Additional Details On Its February 4th Virtual R&D Day

Gain Therapeutics Announces Additional Details On Its February 4th Virtual R&D Day

Neuroscience and Beyond: Harnessing Computational Technology and Allosteric Modulators to Drug the Undruggable BETHESDA, Md., Jan. 31, 2022 (GLOBE NEWSWIRE) -- Gain Therapeutics, Inc. ...

ByGain Therapeutics, Inc.


CD Formulation: Customized Preparation of Active Pharmaceutical Ingredient Excipients to Accelerate Drug Discovery Projects

CD Formulation: Customized Preparation of Active Pharmaceutical Ingredient Excipients to Accelerate Drug Discovery Projects

Excipients usually play important and diversified roles in drugs. They interact with the active pharmaceutical ingredients (APIs) to improve the performance of the drug, for example, to promote drug absorption, to reduce viscosity, or to enhance solubility. ...

ByCD Formulation


AVEO Oncology Presents Three Posters for Tivozanib/Immunotherapy Combinations at the 2022 ASCO GI Cancers Symposium

AVEO Oncology Presents Three Posters for Tivozanib/Immunotherapy Combinations at the 2022 ASCO GI Cancers Symposium

It is a potent, selective inhibitor of VEGFRs 1, 2, and 3 with a long half-life designed to improve efficacy and tolerability. AVEO received U.S. Food and Drug Administration (FDA) approval for FOTIVDA on March 10, 2021 for the treatment of adult patients with relapsed or refractory advanced renal cell carcinoma (RCC) following two or more prior systemic therapies. ...

ByAVEO Pharmaceuticals, Inc.


World Health Organization Panel Strongly Recommends The Use Of Baricitinib To Treat Hospitalised Patients With COVID-19

World Health Organization Panel Strongly Recommends The Use Of Baricitinib To Treat Hospitalised Patients With COVID-19

On Thursday, a panel of WHO experts strongly recommended the janus kinase (JAK) inhibitor baricitinib, a drug owned by Eli Lilly, for patients with severe or critical COVID-19 in combination with corticosteroids. ...

ByBenevolent


AVEO Oncology Highlights Recent Progress and 2022 Outlook

AVEO Oncology Highlights Recent Progress and 2022 Outlook

It is a potent, selective inhibitor of VEGFRs 1, 2, and 3 with a long half-life designed to improve efficacy and tolerability. AVEO received U.S. Food and Drug Administration (FDA) approval for FOTIVDA on March 10, 2021 for the treatment of adult patients with relapsed or refractory advanced renal cell carcinoma (RCC) following two or more prior systemic therapies. ...

ByAVEO Pharmaceuticals, Inc.


Frontier Biotech partners with R-pharm to provide Aikening to Russian patients

Frontier Biotech partners with R-pharm to provide Aikening to Russian patients

Multiple controlled clinical trials and accumulated real-world data show that Aikening® has high efficacy and safety, with minimal drug interactions with commonly used drugs amongst HIV patients and high resistance barriers. ...

ByFrontier Biotechnologies Inc.


Frontier Biotechnologies` First Long-acting Injectable (Aikening(R), in a Two Drug Regimen for HIV, Proves Safe and Efficacious for Patients

Frontier Biotechnologies` First Long-acting Injectable (Aikening(R), in a Two Drug Regimen for HIV, Proves Safe and Efficacious for Patients

The results showed that with a two-drug regimen of ABT (replacing two NRTIs), patients could receive rapid and durable viral suppression for 48 weeks that is not inferior to standard second-line three-drug combination therapy. ...

ByFrontier Biotechnologies Inc.

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