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Innovation in immuno-oncology: Leading companies in in-vitro T-cell activation

Pharmaceutical Technology

In the last three years alone, there have been over 633,000 patents filed and granted in the pharmaceutical industry, according to GlobalData’s report on Immuno-oncology in Pharmaceuticals: In-vitro T-cell activation. Immatics is the leading patent filer in in-vitro T-cell activation.

In-Vitro 130
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Positive in vitro results for Imutex’s FLU-v

Pharma Times

Data further supports the continued development of FLU-v as a broad-spectrum influenza vaccine

In-Vitro 161
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Enanta secures FDA fast track designation for EDP-323 to treat RSV

Pharmaceutical Technology

In vitro data of EDP-323 showed a significant reduction in RSV replication with picomolar potency in primary human bronchial epithelial cells against RSV A and B. We believe this designation will be a valuable component of our clinical and regulatory strategy as we progress EDP-323 in development.”

In-Vitro 276
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TFF and NIEHS partner to develop powder formulations for respiratory diseases

Pharmaceutical Technology

TFF Pharmaceuticals and the National Institute of Environmental Health Sciences (NIEHS) have signed an agreement for the development of dry powder formulations of high molecular weight hyaluronan (HMW-HA) for respiratory diseases.

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Biologic Therapeutics Development, Part 1: Definition and Distinct Characteristics

Camargo

The development of biological products (or biologics) represents a major advancement in modern medicine, enabling the treatment of patients with many illnesses where no other therapeutics were previously available. Small molecules have known structures and are primarily chemically synthesized. ADME and Dosing Regimen.

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Orbit and Evergreen partner to advance radiopharmaceuticals development

Pharmaceutical Technology

Evergreen Discovery has partnered with Orbit Discovery to discover specific cell-targeting peptides and advance the development of new radiopharmaceuticals. The Orbit platform will also conduct in vitro transcription conversion from DNA-encoded libraries on beads.

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World Orphan Drug Congresses Europe vs. The US: Global Perspectives on Genetic Testing

Worldwide Clinical Trials

In-Vitro Diagnostic Regulation and The FDAs Final Rule The WODC U.S. discussion also briefly mentioned the FDAs Final Rule, which seems to run parallel with the EUs In-Vitro Diagnostic Regulation (IVDR). One topic that sparked this dialogue is the potential bankruptcy of 23andMe, a direct-to-consumer genetic testing company.

Genetics 130