Resource Library

A comprehensive library of patient education materials, videos, forms, product information, and resources to support your practice.

Request any of these resources from your Ipsen representative.

Statement of Medical Necessity
IMPORTANT: Be sure to fill out an SMN for each patient so they have access to all the support services of the PACESM (Patient Access, Care & Education) program 		Resources & Reflections Patient Kit
A comprehensive educational kit to address your patients' questions and needs
 
Injection Placemat
Step-by-step guidance for clinic staff on the simple, safe administration of Somatuline® Depot (lanreotide) Injection 		Co-pay program brochures with savings cards
Information for your eligible patients about reducing their co-pays by up to $150 per month*
 
Full Prescribing Information Pocket Dosing Algorithm
Essential information on how to effectively titrate Somatuline Depot for optimal patient response over time
 
Nurse Resource Guide
A booklet to help your staff understand acromegaly and Somatuline Depot therapy 		Administration Video
An instructional video for you and your staff on the convenient administration of Somatuline Depot

*Patient Eligibility Criteria: Patient has been diagnosed with acromegaly. Patient's prescriptions are not paid in part or full by any state-funded or federally funded programs,including but not limited to Medicare, Medicaid, Medigap, VA, DOD, or TriCare. Patient is not a resident of Massachusetts. Starter therapy is available for up to 8 months as long as insurance coverage for Somatuline Depot is actively being pursued by the prescriber and the patient's insurance company has not yet communicated a final coverage decision.

For additional questions or further explanation of our financial assistance and eligibility criteria, please contact PACE at 866-435-5677

Indication and Important Safety Information

  • Somatuline® Depot (lanreotide) Injection is a somatostatin analog indicated for the long-term treatment of patients with acromegaly who have had an inadequate response to or cannot be treated with surgery and/or radiotherapy.

CONTRAINDICATIONS

  • None.

WARNINGS & PRECAUTIONS

  • Somatuline Depot may reduce gallbladder motility and lead to gallstone formation; therefore, patients may need to be monitored periodically.
  • Somatuline Depot and other somatostatin analogs can inhibit the secretion of insulin and glucagon. Patients treated with Somatuline Depot may experience hypoglycemia or hyperglycemia.
  • Antidiabetic treatment may need to be adjusted when Somatuline Depot treatment is initiated or when the dose is altered.
  • Slight decreases in thyroid function have been seen during treatment with Somatuline Depot. Thyroid function tests are recommended where clinically indicated.
  • The most common cardiac adverse reactions observed in patients in 3 pooled cardiac studies were sinus bradycardia (5.5%), bradycardia (2.8%), and hypertension (5.6%).
    • In patients without underlying cardiac disease, Somatuline Depot may lead to a decrease in heart rate without necessarily reaching the threshold of bradycardia.
    • In patients suffering from cardiac disorders prior to Somatuline Depot treatment, sinus bradycardia may occur. Care should be taken when initiating Somatuline Depot treatment in patients with bradycardia.
  • The pharmacological gastrointestinal effects of Somatuline Depot may reduce the intestinal absorption of concomitant drugs.
  • Somatuline Depot may decrease the relative bioavailability of cyclosporine. Cyclosporine dose may need to be adjusted to maintain levels.

SPECIAL POPULATIONS

  • Patients with moderate and severe renal impairment or moderate and severe hepatic impairment should begin treatment with Somatuline Depot 60 mg. Caution should be exercised when considering these patients for an extended dosing interval of Somatuline Depot 120 mg every 6 or 8 weeks.
  • There are no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human responses, Somatuline Depot should be used during pregnancy only if the potential benefit justifies potential risk to the fetus.
  • A decision should be made whether to discontinue nursing or discontinue Somatuline Depot taking into account the importance of the drug to the mother.
  • Patients receiving beta-blockers, calcium channel blockers, or other drugs that affect heart rate may need dose adjustments to those drugs. Somatuline Depot may reduce the intestinal absorption of coadministered drugs. Caution should be used.

ADVERSE EVENTS

  • In pooled studies (N = 416), the most common adverse reactions (incidence > 5%) were diarrhea (37%), cholelithiasis (20%), abdominal pain (19%), nausea (11%), injection–site reaction (9%), constipation (8%), flatulence (7%), headaches (7%), arthralgia (7%),vomiting (7%), and loose stools (6%).
  • Gastrointestinal adverse reactions were mild to moderate and typically resolved within 8 to 10 weeks.
    • 1% of patients in the pooled studies with Somatuline Depot discontinued treatment due to gastrointestinal adverse events.
  • Occasional cases of pancreatitis have been reported.
  • Injection-site pain (4.1%) and injection-site mass (1.7%) were the most frequently reported local adverse reactions.
  • Local side effects were more common at the start of treatment and less common as treatment continued.
    • Injection–site reactions were usually mild to moderate but did lead to withdrawal from clinical studies in two patients.
For Full Prescribing Information, click here.