SKYTROFA is now FDA approved for adults with growth hormone deficiency Learn More
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Getting Started
with SKYTROFA

Whether you’re considering SKYTROFA
or already getting started with treatment, let us help.

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Considering a Growth Hormone Treatment?

As your child's strongest advocate, it's important to explore your treatment options. Talk to your doctor about SKYTROFA to see if it could be the right choice for your child.

Download our discussion guide to help you prepare for that conversation.


3 Steps to Getting Started with SKYTROFA

With SKYTROFA, you’ll receive personalized support every step of the way. From navigating insurance to receiving your SKYTROFA delivery, we're here to guide and assist you throughout your treatment journey.

Step 1:
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Prescription and Enrollment

Once you and your child’s doctor have decided on SKYTROFA as the right treatment option, the HCP will write a prescription and enroll you in the Ascendis Signature Access Program® (A·S·A·P). At that time, a dedicated A·S·A·P Nurse Advocate will be assigned to you.

Step 2:
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Insurance Authorization

Your Nurse Advocate will verify your insurance coverage. Once completed, the Summary of Benefits will be sent to your healthcare provider on the same day.

Step 3:
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Welcome Call with your A·S·A·P Nurse Advocate

Your dedicated Nurse Advocate will reach out to discuss your benefits verification and next steps. This includes:

  • Reviewing insurance coverage and available financial support, if needed
  • Arranging delivery of your SKYTROFA Auto-Injector and Starter Kit
  • Scheduling training on how to use the SKYTROFA Auto-Injector

Ongoing support for your SKYTROFA journey, beyond the first delivery

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Real caregiver of child with GHD

“Our experience with the A·S·A·P program has been phenomenal. It was very reassuring to know we weren’t alone in this process.”

-Nicole, SKYTROFA Caregiver

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Ascendis Signature Access Program® (A·S·A·P) Brochure

For full details on A·S·A·P, download the program brochure to learn more about the personalized patient support available.

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Already started and have questions?

Talk to a member of our support team at 1-844-442-7236 or chat live (available from 8 AM to 8 PM ET, Monday through Friday).

IMPORTANT SAFETY INFORMATION & USES

SKYTROFA is a prescription medicine used for:

  • the replacement of growth hormone in children 1 year old or older who weigh at least 26 pounds (11.5 kilograms) with growth hormone deficiency (GHD)
  • the replacement of growth hormone in adults with growth hormone deficiency (GHD)

Do not take SKYTROFA if:

  • you have a critical illness caused by certain types of heart or stomach surgery, trauma or breathing problems
  • you are allergic to somatropin or any of the ingredients in SKYTROFA

IMPORTANT SAFETY INFORMATION & USES

SKYTROFA is a prescription medicine used for:

  • the replacement of growth hormone in children 1 year old or older who weigh at least 26 pounds (11.5 kilograms) with growth hormone deficiency (GHD)
  • the replacement of growth hormone in adults with growth hormone deficiency (GHD)

Do not take SKYTROFA if:

  • you have a critical illness caused by certain types of heart or stomach surgery, trauma or breathing problems
  • you are allergic to somatropin or any of the ingredients in SKYTROFA
  • you are a child with closed bone growth plates
  • you have cancer or other tumors
  • you have certain types of eye problems caused by diabetes
  • you are a child with Prader-Willi syndrome who is severely obese or has breathing problems including sleep apnea (briefly stopping breathing during sleep)

Tell your healthcare provider if you are pregnant or plan to become pregnant, about all of your medical conditions, and about all the medicines you take. SKYTROFA may affect how other medicines work, and other medicines may affect how SKYTROFA works.

What are the possible side effects of SKYTROFA?

SKYTROFA may cause serious side effects, including:

  • serious allergic reactions. Get medical help right away if you have swelling of the face, mouth, tongue, or throat or trouble breathing
  • high risk of death in people who have critical illnesses caused by heart or stomach surgery, trauma, or serious breathing problems
  • increased risk of growth of an existing tumor or cancer, or increased risk of a previous tumor or cancer returning in people who were treated with radiation to the brain or head as children and who developed low growth hormone problems. Your healthcare provider will need to monitor for the growth or return of a tumor or cancer. Contact your healthcare provider if you start to have sudden changes in behavior, headaches, vision problems, or changes in moles, birthmarks, or skin color
  • new or worsening high blood sugar or diabetes. Your blood sugar may need to be monitored during treatment with SKYTROFA
  • increase in pressure in the skull. Contact your healthcare provider if headaches, eye problems, nausea, or vomiting occur
  • too much fluid in the body (fluid retention). Contact your healthcare provider if you notice swelling in the hands and feet, pain in the joints or muscles, or nerve problems that cause pain, burning or tingling in the hands, arms, legs, and feet
  • decrease in a hormone called cortisol. Your healthcare provider will do blood tests to check your cortisol levels
  • decrease in thyroid hormone levels. Decreased thyroid hormone levels may affect how well SKYTROFA works. Your healthcare provider will do blood tests to check your thyroid hormone levels
  • hip and knee pain or a limp in children (slipped capital femoral epiphysis). This may lead to a serious condition where bone tissue dies due to a lack of blood supply (osteonecrosis). Get medical help right away for children who develop a limp or have hip or knee pain
  • worsening of curvature of the spine in children (scoliosis)
  • severe and constant abdominal pain. This could be a sign of pancreatitis. Tell your healthcare provider about any new abdominal pain
  • loss of fat and tissue weakness in the area of skin you or your child inject. Talk to your healthcare provider about rotating the areas where SKYTROFA is injected
  • high risk of sudden death in children with Prader-Willi syndrome who are severely obese or have breathing problems, including sleep apnea
  • increase in phosphate, alkaline phosphatase, and parathyroid hormone levels in your blood. Your healthcare provider will do blood tests to check this

The most common side effects of SKYTROFA in children include: viral infection, fever, cough, nausea and vomiting, bleeding, diarrhea, stomach area pain, joint pain and arthritis

The most common side effects of SKYTROFA in adults include: swelling due to fluid build-up and low thyroid hormone

These are not all of the possible side effects of SKYTROFA. Call your doctor for medical advice about side effects. You are encouraged to report side effects to FDA at 1-800-FDA-1088 or at www.fda.gov/medwatch. You may also report side effects to Ascendis Pharma at 1-844-442-7236.

Please click here for SKYTROFA full Prescribing Information.