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Manish Gupta

Researcher at Bristol-Myers Squibb

Publications -  41
Citations -  1244

Manish Gupta is an academic researcher from Bristol-Myers Squibb. The author has contributed to research in topics: Nivolumab & Population. The author has an hindex of 15, co-authored 38 publications receiving 998 citations. Previous affiliations of Manish Gupta include University of Tennessee Health Science Center & Children's Hospital of Philadelphia.

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Model-Based Population Pharmacokinetic Analysis of Nivolumab in Patients With Solid Tumors.

TL;DR: A full covariate model was developed to assess covariate effects on pharmacokinetic parameters and found that sex, PS, baseline eGFR, age, race, baseline lactate dehydrogenase, mild hepatic impairment, tumor type, tumor burden, and programmed death ligand‐1 expression had a significant but not clinically relevant (<20%) effect on nivolumab clearance.
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The clinical pharmacokinetics of phosphodiesterase-5 inhibitors for erectile dysfunction.

TL;DR: The major characteristics of the pharmacokinetic profile of all 3 PDE5 inhibitors, including bioavailability and rate of absorption, Biopharmaceutical Classification System categorization, elimination mechanisms, and metabolic profile including active metabolites are discussed.
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The role of pharmacokinetics and pharmacodynamics in phosphodiesterase-5 inhibitor therapy

TL;DR: A critical assessment of the pharmacokinetics of PDE5 inhibitors is provided, which may assist clinicians in tailoring drug and/or treatment regimens to the unique needs of each individual patient with erectile dysfunction.
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Immune Checkpoint inhibitors: An introduction to the next‐generation cancer immunotherapy

TL;DR: The scientific overview of cancer immunotherapy, mechanisms of the inhibitors, clinical pharmacology considerations, advances in combination therapies, and challenges in drug development are discussed.
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Clinical Pharmacology Considerations for the Development of Immune Checkpoint Inhibitors.

TL;DR: The ability of immuno‐oncology to meet its full potential will depend on overcoming development challenges, including the need for clear strategies to determine optimal dose and scheduling for monotherapy as well as combination approaches.