- Signifor LAR
- Signifor: Treatment of Cushing's disease when surgery is not an option or has not resulted in cure
- Signifor LAR: Treatment of acromegaly when surgery is not an option or has not resulted in an adequate response.
Acts as a somatostatin analogue. binding to and activating somatostatin receptors resulting in inhibition of ACTH secretion, which leads to decreased cortisol secretion.
- Improvement in clinical manifestations of Cushing's disease.
- Reduction in growth hormone concentrations and normalization of insulin-like growth factor–1 concentrations.
Distribution: Widely distributed, existing primarily in plasma.
Metabolism and Excretion: Eliminated mainly via hepatic clearance (biliary excretion) with small amounts renally excreted
Half-life: 12 hr.
TIME/ACTION PROFILE (†decrease in urinary free cortisol; ‡ blood levels)
|subcut†||within 1 mo||2 mo||unknown|
- Severe hepatic impairment (Child Pugh C)
- Lactation:Avoid during breastfeeding;
Use Cautiously in:
- Poorly controlled diabetes mellitus (blood sugar should be controlled prior to therapy)
- Cardiac disease and/or risk factors for bradycardia including high-grade heart block, or concomitant use of drugs associated with bradycardia (dose adjustments of beta-blockers, calcium channel blockers, or correction of electrolyte disturbances may be necessary)
- Patients at risk of QT interval prolongation, including congenital long QT prolongation, uncontrolled/significant cardiac disease including recent MI, HF, unstable angina or bradycardia, on antiarrhythmic therapy or other substances that are known to cause QT interval prolongation, hypokalemia and/or hypomagnesemia (correct prior to administration)
- Moderate hepatic impairment (dose ↓ required);
- Geri: Initial lower dose recommended taking into account ↑frequency of altered hepatic, renal, or cardiac function, concomitant diseases or other drug therapy;
- OB: Use during pregnancy only if clearly needed;
- Pedi: Safety and effectiveness not established.
Adverse Reactions/Side Effects
CNS: fatigue, headache, anxiety, dizziness, insomnia, vertigo
CV: BRADYCARDIA, QT INTERVAL PROLONGATION, , hypertension, peripheral edema, hypotension
GI: abdominal pain, anorexia , cholelithiasis, diarrhea, nausea, abdominal distention, constipation, ↑ amylase, ↑ liver enzymes, vomiting
Derm: alopecia, injection site reactions, pruritus
Endo: hyperglycemia, adrenal insufficiency, hypocortisolism, hypoglycemia, pituitary hormone deficiency
F and E: hypokalemia
Hemat: anemia, ↑ prothrombin time
Metabolic: hypercholesterolemia, ↑ lipase
MS: athralgia, back pain, extremity pain, myalgia
* CAPITALS indicate life-threatening.
Underline indicate most frequent.
- Drugs that prolong the QT interval ↑ risk of serious arrhythmias.
- May ↓ absorption and effects of cyclosporine; dose adjustment of cyclosporine may be necessary.
- May ↑ blood levels and effect of bromocriptine (dose ↓ of bromocriptine may be necessary).
- May ↑ blood levels and effects of drugs metabolized by CYP450 enzymes.
SC: (Adults) Initial dose– 0.6 mg or 0.9 mg twice daily (range 0.3–0.9 mg twice daily based on response/tolerability).
(Adults) Moderate hepatic impairment (Child Pugh B)– 0.3 mg twice a day initially (max dose: 0.6 mg twice a day).
IM: (Adults) 40 mg every 4 wk; after 3 mo, if inadequate response, may ↑ to 60 mg every 4 wk.
IM: (Adults) Moderate hepatic impairment (Child Pugh B)– 20 mg every 4 wk; fter 3 mo, if inadequate response, may ↑ to 40 mg every 4 wk.
Solution for subcutaneous injection (Signifor): 0.3 mg/mL, 0.6 mg/mL, 0.9 mg/mL
Powder for intramuscular injection (requires reconstitution) (Signifor LAR): 20 mg/vial, 40 mg/vial, 60 mg/vial
- Obtain a baseline ECG prior to starting and periodically during therapy. Monitor for QT interval prolongation. Correct hypokalemia and hypomagnesemia prior to therapy.
- Perform an ultrasound of the gallbladder prior to therapy and at 6 and 12 mo intervals; cholelithiasis occurs frequently during therapy.
- Monitor for signs and symptoms of hypocortisolism (weakness, fatigue, anorexia, nausea, vomiting, hypotension, hyponatremia, hypoglycemia) periodically during therapy. If hypocortiosolism occurs, may require temporary dose reduction or interruption of therapy and exogenous glucocorticoid replacement.
- Monitor patients with cardiac disease, history of significant bradycardia, high-grade heart block, or those taking drugs that may cause bradycardia for bradycardia. May require dose adjustments of beta blockers, calcium channel blockers, or correction of electrolyte imbalances.
Lab Test Considerations: Monitor fasting plasma glucose, heomglobin A1c and liver tests prior to starting therapy. Blood glucose and or fasting blood glucose should be self-monitored by patient weekly for first 2–3 mo and first 4–6 mo after dose increase, and periodically thereafter. If hyperglycemia occurs, may require initiation or adjustment of hypoglycemic agents.
- Monitor serum electrolytes (potassium, magnesium) prior to and periodically during therapy. Correct hypokelemia and hypomagnesemia before starting therapy and as needed.
- Monitor liver tests after 1–2 wks on therapy, then monthly for 3 months, and every 6 mo thereafter. If ALT is normal at baseline and ↑ of 3–5 times the upper limit of normal occur, repeat test in 1 wk or 48 hrs if >5 time upper limit of normal. If ALT is abnormal at baseline and ↑ of 3–5 times baseline level occur during therapy, repeat test within 1 wk or sooner if >5 time upper limit of normal. If levels are confirmed or rising, interrupt therapy and determine cause. Monitor ALT, AST, alkaline phosphatase, and total bilirubin weekly or more frequently if any level exceeds 5 times baseline level if abnormal baseline or 5 times upper limit of normal if baseline normal. If abnormalities resolve, resume therapy cautiously and monitor closely.
- Monitor pituitary function (TSH/free T4, GH/IGF-1) prior to starting and periodically during therapy.
- May cause asymptomatic and reversible ↑ in amylase and lipase.
- May cause slight ↓ in hemoglobin and minimal ↑ in PT and PTT.
- Deficient knowledge, related to disease process and medication regimen (Patient/Family/Teaching)
- SC: Pinch skin and inject at 45° angle into top of thigh or abdomen. Place cotton ball or alcohol wipe over injection site and press for 5 seconds. Do not massage. Rotate sites; do not administer into site that is red or irritated. Solution is clear and colorless, do not inject solutions that are discolored or contain a precipitate.
- IM: Allow vial to reach room temperature for at least 30 min, but not more than 24 hrs. Reconstitute with 2 mL diluent provided by manufacturer following manufacturer's instructions. Concentration: 10 mg/mL, 20 mg/mL, or 30 mg/mL based on dose.Shake vial moderately in horizontal position for at least 30 seconds until uniform suspension is formed; repeat shaking until all powder is completely suspended. Do not administer suspensions that are discolored or contain particulate matter. Inject slowly at a 90° angle into left or right gluteus. Missed dose may be given up until 14 days before next scheduled dose.
- Instruct patient in correct technique for injection, care and disposal of equipment. Advise patient to read Medication Guide prior to using and with each Rx refill, in case of changes.
- Advise patient to notify health care professional if signs and symptoms of hypocortisolism and hyperglycemia (excessive thirst, high urine output, increased appetite with weight loss, tiredness) occur.
- Advise patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and to consult with health care professional before taking other medications
- Advise female patient to notify health care professional if pregnancy is planned or suspected or if breastfeeding.
- Reduction in 24-hour urinary free cortisol (UFC), typically seen in 2 mo.
- Improvement in signs and symptoms of Cushing's disease.
- Reduction in growth hormone concentrations and normalization of insulin-like growth factor–1 concentrations in patients with acromegaly.
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