Hear directly from endocrinologists and patients about their CRENESSITY experience

Meet 3 CAH specialists

These providers talk about the challenges of treating CAH and their recent experiences prescribing CRENESSITY.

Select an endocrinologist’s image to learn more.

Stay tuned for upcoming videos to see these endocrinologists reflect on treating classic CAH with CRENESSITY.

A lot of patients do come in, and they say, ‘Hey, what about this drug?’ This is an exciting opportunity to be able to give them something different, which we didn’t have before.”

Dr. Heidi SheaAdult & Pediatric EndocrinologistCompensated by Neurocrine for sharing her views.

CLINICAL PROFILES FROM THE CAHTALYST™ TRIALS

Kristy & Grant

Kristy shares her son Grant’s experience with CRENESSITY during the clinical trial—and beyond—including how much his androgen levels and GC dose dropped.

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Clinical Profiles

Kristy & Grant

Clinical Profiles

Susan

Clinical Profiles

Paul

Clinical Profiles

Liam

Ambassadors were compensated by Neurocrine for sharing their stories.

SCIENCE OF CRENESSITY

Mechanism of Action

Watch the video to learn more about how CRENESSITY works in the CRF pathway.

Dosing

Review the dosing and administration information for CRENESSITY.

Support & Resources

Review dedicated support for you and your patients.

CAH=congenital adrenal hyperplasia; CRF=corticotropin-releasing factor; GC=glucocorticoid.

INDICATION

CRENESSITY (crinecerfont) is indicated as adjunctive treatment to glucocorticoid replacement to control androgens in adults and pediatric patients 4 years of age and older with classic congenital adrenal hyperplasia (CAH).

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

CRENESSITY is contraindicated in patients with hypersensitivity to crinecerfont or any excipients of CRENESSITY.

WARNINGS AND PRECAUTIONS

Hypersensitivity Reactions. A hypersensitivity reaction, including throat tightness, angioedema, and generalized rash, occurred in a subject after 3 days of treatment with CRENESSITY. If a clinically significant hypersensitivity reaction occurs, initiate appropriate therapy and discontinue CRENESSITY.

Risk of Acute Adrenal Insufficiency or Adrenal Crisis with Inadequate Concomitant Glucocorticoid Therapy. Acute adrenal insufficiency or adrenal crisis, which is potentially life-threatening, can occur in patients with underlying adrenal insufficiency who are on inadequate daily glucocorticoid doses, especially in situations associated with increased cortisol need, such as acute intercurrent illness, serious trauma, or surgical procedures. Continue glucocorticoids upon initiation of and during treatment with CRENESSITY. Do not reduce the glucocorticoid dose below the dose required for cortisol replacement. Patients should continue to use stress dosing of glucocorticoids in cases of increased cortisol need.

ADVERSE REACTIONS

In adult patients, the most common adverse reactions (at least 4% for CRENESSITY and greater than placebo) are fatigue, headache, dizziness, arthralgia, back pain, decreased appetite, and myalgia.

In pediatric patients, the most common adverse reactions (at least 4% for CRENESSITY and greater than placebo) are headache, abdominal pain, fatigue, nasal congestion, and epistaxis.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit MedWatch at www.fda.gov/medwatch or call 1-800-FDA-1088.

Dosage Forms and Strengths:

CRENESSITY is available in 50 mg and 100 mg capsules, and as an oral solution of 50 mg/mL.

Please see full Prescribing Information.