SUPPORT & SERVICES

AMRYT Assist: Comprehensive Support and Access Made Easy

Designed to guide patients with acromegaly through starting
and staying on MYCAPSSA

Financial assistance

including copay assistance for eligible patients and referrals to other sources of support

Benefits investigation

to understand your patients’ insurance coverage for MYCAPSSA and how we can help

Specialty pharmacy interaction

to ensure set-up and delivery at the right place and time

Patient assistance program

for individuals without insurance or who meet other eligibility requirements

Learn more about how eligible, commercially insured patients can get MYCAPSSA for as little as

$0 OUT OF POCKET

We’re Ready to Assist Your Office and Patients Today

That way, consistent control for acromegaly can be in your patients’ hands with daily oral MYCAPSSA.

Call Amryt Assist with any questions at 1-833-346-2277 (Monday–Friday, 8:30AM-7:00PM EST).

You can also access the prescription and enrollment forms below to begin the process, and make access to MYCAPSSA as seamless as possible for your patients.

Download Enrollment Form

Includes Prescription and Patient Consent

Interested in learning more?

Let us know how we can help:

I'd like to request a visit or schedule a conversation with an Amryt Rare Disease Specialist.

I'd like to receive additional information and resources for MYCAPSSA.

# of patients with acromegaly*

# of acromegaly patients managed*

*Required Field

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INDICATION AND IMPORTANT SAFETY INFORMATION

INDICATION AND USAGE
MYCAPSSA (octreotide) delayed-release capsules, for oral use, is a somatostatin analog indicated for long-term maintenance treatment in acromegaly patients who have responded to and tolerated treatment with octreotide or lanreotide.

CONTRAINDICATIONS
Hypersensitivity to octreotide or any of the components of MYCAPSSA. Anaphylactoid reactions, including anaphylactic shock, have been reported in patients receiving octreotide.

WARNINGS AND PRECAUTIONS
MYCAPSSA can cause problems with the gallbladder. Monitor patients periodically. Discontinue if complications of cholelithiasis are suspected.

Blood sugar, thyroid levels, and vitamin B₁₂levels should be monitored and treated accordingly.

Bradycardia, arrhythmia, or conduction abnormalities may occur. Treatment with drugs that have bradycardia effects may need to be adjusted.

ADVERSE REACTIONS
The most common adverse reactions (incidence >10%) are nausea, diarrhea, headache, arthralgia, asthenia, hyperhidrosis, peripheral swelling, blood glucose increased, vomiting, abdominal discomfort, dyspepsia, sinusitis, and osteoarthritis.

DRUG INTERACTIONS
The following drugs require monitoring and possible dose adjustment when used with MYCAPSSA: cyclosporine, insulin, antidiabetic drugs, calcium channel blockers, beta blockers, lisinopril, digoxin, bromocriptine, and drugs mainly metabolized by CYP3A4. Counsel women taking an oral contraceptive to use an alternative non-hormonal method of contraception or a back-up method when taking MYCAPSSA.

Patients taking proton pump inhibitors, H2-receptor antagonists, or antacids concomitantly with MYCAPSSA may require increased dosages of MYCAPSSA.

PREGNANCY
Advise premenopausal females of the potential for an unintended pregnancy.

To report SUSPECTED ADVERSE REACTIONS, contact the product information department at 1-844-312-2462 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch