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A new compound shows promise as a topical treatment for hair loss.

Finasteride's two formulations absorb similarly, showing bioequivalence.

Different drugs can treat high male hormone levels in women, but they have various effects and some may harm a fetus.

Scientists created iodinated arylhydantoins and arylthiohydantoins that could potentially be used for imaging prostate cancer. Some versions with specific side-chains showed high potential for this use.

Scientists made new substances that can block an enzyme linked to prostate issues and hair loss, with potential for creating a new treatment.

Using tissue adhesive in hair transplants improves results and patient satisfaction, with fewer complications.

KATP channels are important for energy balance and are targeted by drugs for diabetes, hypoglycemia, hypertension, and hair loss.

Women with PCOS who have high male hormone levels often also have insulin resistance.

BeauTop improves hair growth in androgenetic alopecia patients.

5α-reductase inhibitors help treat disorders caused by DHT and have potential for future therapies.

Certain amino acid analogues can inhibit wool and hair growth and affect fiber strength.

Anti-androgens are effective for female acne but less so for male-pattern hair loss, with side effects similar to birth control pills.

Granules improve hair loss treatment by targeting follicles.

Hesperidin protects rat testicles from finasteride damage and improves sperm health.

A new, less toxic and more efficient method to create the anti-baldness compound RU58841 was developed in 2014.

Researchers made two new compounds that could be used for medicine.

The mesenchymal stem cell-conditioned medium gel improved burn healing and hair growth in rats better than other treatments.

Dates may improve heart health, fight infections, protect kidneys, reduce inflammation, support pregnancy, promote dental and bone health, enhance mental function, and have anti-cancer properties, and are also beneficial for skin and hair care.

A new method was created to test the effectiveness of Dihydrotestosterone (DHT) inhibitors, like finasteride and dutasteride, in human and fish cells. The results showed fish cells are more sensitive to these treatments, and dutasteride works better than finasteride in all tested cells.

5α-reductase inhibitors don't stop bladder cancer from developing or getting worse.

Aleglitazar and its major metabolite are safe enough to proceed to Phase 3 clinical trials.

Taking five small dutasteride capsules is the same as taking one larger capsule.

Fermentation of Finasteride with Ocimum sanctum L. creates new metabolite that inhibits tyrosinase.

Scientists made a carbon-14 labeled version of a drug with a 48% yield and over 99% purity.

TS-13 effectively stops tumor growth and reduces chemotherapy side effects.

The conclusion is that analyzing RNA from skin oils is a promising way to understand skin diseases.

Flutamide-induced hypospadias in rats slows down early wound healing.

The developed model can predict effective 5-alpha-reductase enzyme inhibitors.

Finasteride metabolites found in pigs match human studies, making pigs a valid model for human drug research.