Our clinical trials of tildacerfont in adults with classic CAH, CAHmelia 203 and CAHmelia 204, are open for screening | LEARN MORE


Classic CAH is a chronic and potentially life-threatening rare genetic disorder characterized by an inability to produce cortisol, and, in many CAH patients, an inability to produce aldosterone. Due to the severity of the disease, most developed countries have established newborn screening programs to test for classic CAH at birth. There are approximately 20,000 – 30,000 classic CAH patients in the U.S. and 50,000 in the EU. There have been no meaningful improvements in CAH treatments in approximately 50 years.

Cortisol is a vital hormone, often called the stress hormone, and acts to prevent the release of substances in the body that cause inflammation, and also to stabilize blood sugar levels. Without cortisol, patients confront the potential for life-threatening adrenal crisis. Aldosterone is also a critical hormone, essential for sodium and potassium level regulation, and hence for control of blood pressure. The inability in CAH to produce cortisol has a key secondary effect, which is significant overproduction of adrenal androgens.

All patients require lifelong treatments with glucocorticoids to replace the missing cortisol and avoid adrenal crisis. But replacement of cortisol alone does not manage the disease: It is estimated that approximately 70% of adult classic CAH patients are living with disease that is considered poorly controlled, primarily because they have adrenal hormones outside of the normal range.1 With limited options currently available, many patients may be prescribed excessive doses of glucocorticoids to reduce high levels of adrenal androgens.

1 Sources: Back Bay Physician Interviews; Horm Res Paediatr 2011;76:73–85, Nat Rev Endocrinol. 2014 Feb;10(2):115-24.

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Clinical management of adult classic CAH is a difficult balance between reducing excessive doses of glucocorticoids or reducing adrenal androgen levels

Replacement Glucocorticoid Steroids
and Excessive Adrenal Androgens
Excessive Glucocorticoid Steroids
and Reduced Adrenal Androgens

The challenges of living with elevated adrenal androgens or excessive glucocorticoid use

Excess adrenal androgens can lead to challenging and often lifelong health issues for classic CAH patients, including premature puberty, impaired fertility in both sexes, excess body hair growth, male pattern balding, acne, menstrual irregularities in women, and testicular adrenal rest tumors (TARTs) in men.

Chronic use of excessive steroids requires careful management due to the well-known serious side effects, which include growth inhibition in children, high blood pressure and high cholesterol, obesity, diabetes, osteoporosis, muscle weakness, psychological effects, skin thinning, and increased risks of infections.

Excess Adrenal Androgens
Psychological Effects
Hirsutism, amenorrhea
Short Stature
Abnormal and/or early puberty
Excess Glucocorticoid Steroids
Psychological Effects
Insulin Resistance
Short Stature

Tildacerfont, by potentially controlling excess adrenal androgens through an independent mechanism, may reduce the clinical symptoms associated with high androgen exposure and enable treating physicians to lower glucocorticoid doses to near physiologic replacement levels.


Tildacerfont is an investigational product and is not FDA approved.