Drug intelligence / Profile preview

letrozole + ubidecarenone

Development stage
Unknown
Lead developer
Novartis
Modality
Small Molecules
Administration
Oral
01

Overview

letrozole + ubidecarenone is a combination of a pharmaceutical aromatase inhibitor (letrozole) and a dietary supplement/cofactor (ubidecarenone, also known as coenzyme Q10). **Letrozole** is a non-steroidal aromatase inhibitor that blocks estrogen production by competitively inhibiting CYP19A1, reducing the conversion of androgens to estrogens. It is primarily indicated for hormone receptor-positive breast cancer in postmenopausal women but is also used off-label for ovulation induction in infertility, including polycystic ovary syndrome (PCOS). **Ubidecarenone (coenzyme Q10)** is a naturally occurring essential cofactor in the mitochondrial electron transport chain, mediating electron transfer between complexes I/II and III to facilitate ATP production. Ubidecarenone also has antioxidant properties, helping to protect membranes against lipid peroxidation and oxidative stress. Clinical research and clinicaltrials suggest the combination of letrozole with ubidecarenone (as coenzyme Q10) may be investigated for uses such as infertility, notably male and female infertility, but it is not an approved or widely marketed co-packaged drug. Letrozole is developed and marketed by major pharmaceutical companies for cancer and infertility, while ubidecarenone is manufactured as a dietary supplement by many companies; their combination is investigational, and development status is most relevant in the context of clinical trials for infertility.

02

Targets

NADH:ubiquinone oxidoreductase subunit familySDH (Mitochondrial electron transport chain complex II)CYP19A1 (Aromatase)Mitochondrial complex III quinone-binding sites

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