Academia and industry agreement on a feasibility tool for first‐time‐in‐human clinical trial units
Abstract First‐time‐in‐human (FTIH) trials are designed to generate information on the safety, tolerability, as well as the pharmacokinetic and pharmacodynamics profile of new drugs. To ensure the safety of participants, these trials need to be conducted at specifically equipped phase I clinical tri...
Main Authors: | , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2023-12-01
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Series: | Clinical and Translational Science |
Online Access: | https://doi.org/10.1111/cts.13655 |