Sun.Dec 29, 2024

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Too Much Sitting Can Still Be Harmful Even if You Exercise, Study Warns

AuroBlog - Aurous Healthcare Clinical Trials blog

(Dave & Les Jacobs/DigitalVision/Getty Images) We know that too much sitting is bad for us, but a new study adds an important detail: if you spend more than 10-and-a-half hours a day sitting or lying down, regular exercise might not be enough to prevent an increased risk of serious heart issues.

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Nelistotug by GSK for Recurrent Head And Neck Squamous Cell Carcinoma: Likelihood of Approval

Pharmaceutical Technology

Nelistotug is under clinical development by GSK and currently in Phase II for Recurrent Head And Neck Squamous Cell Carcinoma.

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Drug Patent Expirations for the Week of December 29, 2024

Drug Patent Watch

FENTORA (fentanyl citrate) Cephalon Patent: 8,119,158 Expiration: Dec 30, 2024 See More … For more information on how DrugPatentWatch can help with your pharmaceutical business intelligence needs, contact admin@DrugPatentWatch.com or visit www.DrugPatentWatch.

Drugs 52
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Trastuzumab rezetecan by Jiangsu Hengrui Medicine for Head And Neck Cancer: Likelihood of Approval

Pharmaceutical Technology

Trastuzumab rezetecan is under clinical development by Jiangsu Hengrui Medicine and currently in Phase I for Head And Neck Cancer.

Medicine 100
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From Diagnosis to Delivery: How AI is Revolutionizing the Patient Experience

Speaker: Simran Kaur, Founder & CEO at Tattva Health Inc.

The healthcare landscape is being revolutionized by AI and cutting-edge digital technologies, reshaping how patients receive care and interact with providers. In this webinar led by Simran Kaur, we will explore how AI-driven solutions are enhancing patient communication, improving care quality, and empowering preventive and predictive medicine. You'll also learn how AI is streamlining healthcare processes, helping providers offer more efficient, personalized care and enabling faster, data-driven

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PDMA seeks PM’s intervention to extend time for MSMEs to comply with Revised GMP standards

AuroBlog - Aurous Healthcare Clinical Trials blog

The Punjab Drug Manufacturers Association (PDMA) has requested Prime Minister Narendra Modi to give more time to the micro and small units under Rs. 10 crore, who have not availed tax holiday benefits, for at least three years to comply with the Revised Schedule M standards.

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Trastuzumab rezetecan by Jiangsu Hengrui Medicine for Transitional Cell Carcinoma (Urothelial Cell Carcinoma): Likelihood of Approval

Pharmaceutical Technology

Trastuzumab rezetecan is under clinical development by Jiangsu Hengrui Medicine and currently in Phase I for Transitional Cell Carcinoma (Urothelial Cell Carcinoma).

Medicine 100

More Trending

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GCC-4001 by Artiva Biotherapeutics for Diffuse Large B-Cell Lymphoma: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Diffuse Large B-Cell Lymphoma.

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GCC-4001 by Artiva Biotherapeutics for Lupus Nephritis: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase I for Lupus Nephritis.

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GCC-4001 by Artiva Biotherapeutics for Follicular Lymphoma: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Follicular Lymphoma.

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GCC-4001 by Artiva Biotherapeutics for Waldenstrom Macroglobulinemia (Lymphoplasmacytic Lymphoma): Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Waldenstrom Macroglobulinemia (Lymphoplasmacytic Lymphoma).

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Optimizing Clinical Supply Strategy: Navigating Challenges & Finding Your Ideal Model

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GCC-4001 by Artiva Biotherapeutics for Angioimmunoblastic T-Cell Lymphoma (AITL)/Immunoblastic Lymphadenopathy: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Angioimmunoblastic T-Cell Lymphoma (AITL)/Immunoblastic Lymphadenopathy.

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GCC-4001 by Artiva Biotherapeutics for Peripheral T-Cell Lymphomas (PTCL): Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Peripheral T-Cell Lymphomas (PTCL).

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Nelistotug by GSK for Recurrent Head And Neck Squamous Cell Carcinoma: Likelihood of Approval

Pharmaceutical Technology

Nelistotug is under clinical development by GSK and currently in Phase II for Recurrent Head And Neck Squamous Cell Carcinoma.

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Trastuzumab rezetecan by Jiangsu Hengrui Medicine for Head And Neck Cancer: Likelihood of Approval

Pharmaceutical Technology

Trastuzumab rezetecan is under clinical development by Jiangsu Hengrui Medicine and currently in Phase I for Head And Neck Cancer.

Medicine 100
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The New Age of Decentralized Clinical Trials

White paper that delves into the complex topic of Decentralized Clinical Trials and how to master them within the confines of FDA Regulations

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Trastuzumab rezetecan by Jiangsu Hengrui Medicine for Transitional Cell Carcinoma (Urothelial Cell Carcinoma): Likelihood of Approval

Pharmaceutical Technology

Trastuzumab rezetecan is under clinical development by Jiangsu Hengrui Medicine and currently in Phase I for Transitional Cell Carcinoma (Urothelial Cell Carcinoma).

Medicine 100
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GCC-4001 by Artiva Biotherapeutics for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma): Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma).

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GCC-4001 by Artiva Biotherapeutics for Diffuse Large B-Cell Lymphoma: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Diffuse Large B-Cell Lymphoma.

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GCC-4001 by Artiva Biotherapeutics for Lupus Nephritis: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase I for Lupus Nephritis.

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European Clinical Supply Planning: Balancing Cost, Flexibility and Time

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GCC-4001 by Artiva Biotherapeutics for Follicular Lymphoma: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Follicular Lymphoma.

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GCC-4001 by Artiva Biotherapeutics for Waldenstrom Macroglobulinemia (Lymphoplasmacytic Lymphoma): Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Waldenstrom Macroglobulinemia (Lymphoplasmacytic Lymphoma).

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GCC-4001 by Artiva Biotherapeutics for Angioimmunoblastic T-Cell Lymphoma (AITL)/Immunoblastic Lymphadenopathy: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Angioimmunoblastic T-Cell Lymphoma (AITL)/Immunoblastic Lymphadenopathy.

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GCC-4001 by Artiva Biotherapeutics for Peripheral T-Cell Lymphomas (PTCL): Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Peripheral T-Cell Lymphomas (PTCL).

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The New Age of Decentralized Clinical Trials

This new white paper defines and details the impact of Decentralized Clinical Trials on the Pharmaceutical industry and how the impact can be measured along with steps companies can take to ensure adoption.