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Enobosarm significantly increased muscle mass and improved physical function in elderly men and postmenopausal women without serious side effects.

Dutasteride is as safe for the heart as finasteride.

Finasteride 1mg linked to diverse symptoms; other treatments improve erectile function in rats.

The new hair product quickly reduces hair shedding in women.

The drug combination was safe and showed promise in treating advanced tumors.

Dutasteride is safe and effective for treating hair loss, but may decrease libido.

Minoxidil is a new drug that lowers blood pressure.

Low-dose dutasteride effectively and safely promotes hair growth in men with androgenetic alopecia.

Minoxidil effectively treats severe hypertension but may cause side effects, so careful monitoring is needed.

Some herbs show promise as antiandrogenic agents.

5-alpha reductase inhibitors can cause sexual side effects like erectile dysfunction, but the exact reasons are unclear.

Finasteride and dutasteride both increase chromogranin A levels similarly.

Finasteride doesn't affect erections much, but may decrease libido in men.

MK-386 and finasteride together effectively reduce DHT levels, potentially treating acne and male pattern baldness.

A new compound with strong antiandrogenic effects was found, potentially useful for treating conditions like acne and prostate cancer.

Finasteride effectively reduces DHT and E2 levels, helping with prostate enlargement.

Finasteride may help reduce inappropriate sexual behaviors in dementia patients with prostate issues.

Finasteride improves heart function in obese and aging male rats by reducing oxidative stress and p53 protein levels.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

The model successfully predicted new uses for existing drugs, like using certain hormonal and heart medications for respiratory and Parkinson's diseases, and a cancer drug for diabetes.

Canagliflozin helps overcome progestin resistance in certain endometrial cancer cells.

The study created a new method to test drugs that affect hormone processing in skin.

5α-reductase inhibitors can cause serious and possibly lasting sexual and psychological side effects.

Urotensin II increases growth and VEGF production in rat skin cells by turning on the Wnt-β-catenin pathway.

Combination therapy improves urinary flow and reduces residual urine, but needs better stent design.