A Phase 1 Study to Investigate the Effects of Cortexolone 17 alpha-Propionate, Also Known as Clascoterone, on the QT Interval Using the Meal Effect to Demonstrate ECG Assay Sensitivity
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A Phase 1 Study to Investigate the Effects of Cortexolone 17 alpha-Propionate, Also Known as Clascoterone, on the QT Interval Using the Meal Effect to Demonstrate ECG Assay Sensitivity. / Taubel, Jorg; Mazzetti, Alessandro; Ferber, Georg; Burch, William; Fernandes, Sara; Patel, Avani; Spencer, Christopher S.; Freier, Anne; Graff, Claus; Kanters, Jorgen K.; Camm, John.
In: Clinical Pharmacology in Drug Development, Vol. 10, No. 6, 2021, p. 572-581.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - A Phase 1 Study to Investigate the Effects of Cortexolone 17 alpha-Propionate, Also Known as Clascoterone, on the QT Interval Using the Meal Effect to Demonstrate ECG Assay Sensitivity
AU - Taubel, Jorg
AU - Mazzetti, Alessandro
AU - Ferber, Georg
AU - Burch, William
AU - Fernandes, Sara
AU - Patel, Avani
AU - Spencer, Christopher S.
AU - Freier, Anne
AU - Graff, Claus
AU - Kanters, Jorgen K.
AU - Camm, John
PY - 2021
Y1 - 2021
N2 - Cortexolone 17 alpha-propionate, also known as clascoterone, is a potent androgen receptor inhibitor intended for the topical treatment of skin diseases associated with androgenic pathway alterations. In nonclinical studies, cortexolone 17 alpha-propionate was found to have a weak inhibitory effect on human Ether-a-go-go-Related Gene (hERG) potassium channels, which are vital for normal electrical activity in the heart. When used in a cream formulation, little cortexolone 17 alpha-propionate is absorbed. However, the solution formulation developed for the treatment of androgenetic alopecia leads to a measurable systemic concentration and accumulation of the antiandrogen. This phase 1 study assessed the effect of cortexolone 17 alpha-propionate on the QTc interval using concentration-effect analysis and the effect of a meal on QTc to confirm assay sensitivity. Thirty-two volunteers were randomly assigned to receive the active drug or a matching vehicle as placebo. Participants were dosed twice daily on days 1 to 3 (225 mg applied topically as a 7.5% solution 12 hours apart) and once on day 4. Pharmacokinetic and electrocardiogram assessments were performed after supratherapeutic doses. Assay sensitivity was successfully confirmed by using the food effect on the QTc interval. The results of this concentration-QTc analysis demonstrate that cortexolone 17 alpha-propionate and its metabolite/degradation product had no effect on the QTc interval in the concentration range tested.
AB - Cortexolone 17 alpha-propionate, also known as clascoterone, is a potent androgen receptor inhibitor intended for the topical treatment of skin diseases associated with androgenic pathway alterations. In nonclinical studies, cortexolone 17 alpha-propionate was found to have a weak inhibitory effect on human Ether-a-go-go-Related Gene (hERG) potassium channels, which are vital for normal electrical activity in the heart. When used in a cream formulation, little cortexolone 17 alpha-propionate is absorbed. However, the solution formulation developed for the treatment of androgenetic alopecia leads to a measurable systemic concentration and accumulation of the antiandrogen. This phase 1 study assessed the effect of cortexolone 17 alpha-propionate on the QTc interval using concentration-effect analysis and the effect of a meal on QTc to confirm assay sensitivity. Thirty-two volunteers were randomly assigned to receive the active drug or a matching vehicle as placebo. Participants were dosed twice daily on days 1 to 3 (225 mg applied topically as a 7.5% solution 12 hours apart) and once on day 4. Pharmacokinetic and electrocardiogram assessments were performed after supratherapeutic doses. Assay sensitivity was successfully confirmed by using the food effect on the QTc interval. The results of this concentration-QTc analysis demonstrate that cortexolone 17 alpha-propionate and its metabolite/degradation product had no effect on the QTc interval in the concentration range tested.
KW - androgen receptor inhibitor
KW - androgenetic alopecia
KW - antiandrogen
KW - cardiac safety
KW - cortexolone 17α
KW - ‐
KW - propionate
KW - QT interval
KW - ANTIANDROGEN
KW - TIME
U2 - 10.1002/cpdd.935
DO - 10.1002/cpdd.935
M3 - Journal article
C2 - 33942574
VL - 10
SP - 572
EP - 581
JO - Clinical Pharmacology in Drug Development
JF - Clinical Pharmacology in Drug Development
SN - 2160-763X
IS - 6
ER -
ID: 286848649