Dataset Information

Evolution of Ritlecitinib Population Pharmacokinetic Models During Clinical Drug Development.

ABSTRACT:

Background

Ritlecitinib is an oral Janus kinase 3/tyrosine kinase expressed in hepatocellular carcinoma family inhibitor undergoing parallel clinical development for alopecia areata, vitiligo, ulcerative colitis, Crohn's disease, and rheumatoid arthritis.

Objective

As studies read out simultaneously, strategic planning of population pharmacokinetic model development and evaluation is required to ensure timely decisions.

Methods

Data from healthy participants and patients from 12 clinical trials between December 2014 and July 2021 were included: seven phase I studies in healthy participants and organ impairment, five phase II/III studies in patients with rheumatoid arthritis, ulcerative colitis, alopecia areata, and vitiligo. Population pharmacokinetic models consisted of stepwise procedures to accommodate data availability and the model's application to answering clinical development questions. At each iteration of the model update, parameters of the next model were re-estimated by leveraging previous information and new data.

Results

Three model development lifecycle iterations of the ritlecitinib population pharmacokinetic model were conducted to support alopecia areata, vitiligo, and ulcerative colitis study readouts. Initial structural modeling based on healthy participant data (and some rheumatoid arthritis and alopecia areata data) in iteration 1 provided a platform for comprehensive covariate testing during iteration 2, and model evaluation and implementation of the frequentist prior approach in iteration 3. The final model was a two-compartment model with first-order absorption and direct-response non-stationary clearance and bioavailability driven by concentrations in the peripheral compartment.

Conclusions

The present approach demonstrated the evolution of three population pharmacokinetic models with accumulating data, addressed clinical drug development questions related to systemic exposures of ritlecitinib, and informed the approved product label.

Clinical trial registration

NCT02309827, NCT02684760, NCT02958865, NCT02969044, NCT03232905, NCT03732807, NCT04016077, NCT03715829, NCT04037865, NCT04004663, NCT04634565, NCT02974868.

SUBMITTER: Wojciechowski J

PROVIDER: S-EPMC10684409 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature

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Publications

Evolution of Ritlecitinib Population Pharmacokinetic Models During Clinical Drug Development.

Wojciechowski Jessica J S Purohit Vivek V Huh Yeamin Y Banfield Christopher C Nicholas Timothy T

Clinical pharmacokinetics 20231102 12

<h4>Background</h4>Ritlecitinib is an oral Janus kinase 3/tyrosine kinase expressed in hepatocellular carcinoma family inhibitor undergoing parallel clinical development for alopecia areata, vitiligo, ulcerative colitis, Crohn's disease, and rheumatoid arthritis.<h4>Objective</h4>As studies read out simultaneously, strategic planning of population pharmacokinetic model development and evaluation is required to ensure timely decisions.<h4>Methods</h4>Data from healthy participants and patients fr ...[more]

PMID: 37917289

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Dataset Information

Evolution of Ritlecitinib Population Pharmacokinetic Models During Clinical Drug Development.

Background

Objective

Methods

Results

Conclusions

Clinical trial registration

Publications

Evolution of Ritlecitinib Population Pharmacokinetic Models During Clinical Drug Development.

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