Gavreto

— THERAPEUTIC DISORDERS TREATED —
  • Pancreatic, thyroid, and other endocrine cancers
  • Respiratory and thoracic cancers

Gavreto Generic Name & Formulations

General Description

Pralsetinib 100mg; caps.

Pharmacological Class

Kinase inhibitor.

How Supplied

Caps—60, 90, 120

Generic Availability

NO

Gavreto Indications

Indications

Advanced or metastatic RET-mutant medullary thyroid cancer (MTC) in patients who require systemic therapy. Advanced or metastatic RET fusion-positive thyroid cancer in patients who require systemic therapy and who are radioactive iodine-refractory (if radioactive iodine is appropriate).

Gavreto Dosage and Administration

Adult

Confirm presence of a RET gene fusion or mutation. Take on an empty stomach. ≥12yrs: 400mg once daily. Continue until disease progression or until unacceptable toxicity. Concomitant use with combined P-gp and strong CYP3A inhibitors (if unavoidable): reduce to 200mg once daily if current dose is 300mg or 400mg once daily; reduce dose to 100mg once daily if current dose is 200mg once daily. Concomitant use with strong CYP3A inducers (if unavoidable): increase initial dose to double the current Gavreto dosage starting on Day 7 of concomitant use. Dose modifications for adverse reactions: see full labeling.

Children

<12yrs: not established.

Gavreto Contraindications

Not Applicable

Gavreto Boxed Warnings

Not Applicable

Gavreto Warnings/Precautions

Warnings/Precautions

Monitor for pulmonary symptoms indicative of ILD/pneumonitis; withhold therapy and evaluate if occurs. Uncontrolled hypertension: do not initiate. Optimize BP prior to initiation; monitor after 1 week, then at least monthly thereafter and as clinically indicated. Hepatotoxicity. Monitor AST/ALT prior to initiation, every 2 weeks during 1st 3 months, then monthly thereafter and as clinically indicated. Permanently discontinue if severe or life-threatening hemorrhagic events occur. Risk of tumor lysis syndrome in those with MTC (esp. with rapidly growing tumors, high tumor burden, renal dysfunction, dehydration); monitor. Risk of impaired wound healing: withhold for ≥5 days prior to elective surgery; do not give for ≥2 weeks after major surgery and until adequate healing. Moderate (total bilirubin >1.5–3.0×ULN and any AST) or severe (total bilirubin >3.0×ULN and any AST) hepatic impairment. Embryo-fetal toxicity. Advise to use effective non-hormonal contraception during and for 2 weeks (females of reproductive potential) or 1 week (males w. female partners) after the last dose. Pregnancy: exclude status prior to initiation. Nursing mothers: not recommended (during and for 1 week after the last dose).

Gavreto Pharmacokinetics

See Literature

Gavreto Interactions

Interactions

See Adults. Potentiated by strong CYP3A inhibitors. Avoid concomitant combined P-gp and strong CYP3A inhibitors; if unavoidable, reduce Gavreto dose. Antagonized by strong CYP3A inducers; avoid concomitant use; if unavoidable, increase Gavreto dose. May antagonist hormonal contraceptives.

Gavreto Adverse Reactions

Adverse Reactions

Constipation, hypertension, fatigue, musculoskeletal pain, diarrhea; laboratory abnormalities (decreased lymphocytes, decreased neutrophils, decreased hemoglobin, decreased phosphate, decreased sodium, decreased calcium [corrected], increased ALT/AST/alkaline phosphatase, decreased platelets), pneumonia, pneumonitis, sepsis, UTI, pyrexia.

Gavreto Clinical Trials

See Literature

Gavreto Note

Not Applicable

Gavreto Patient Counseling

See Literature

Gavreto Generic Name & Formulations

General Description

Pralsetinib 100mg; caps.

Pharmacological Class

Kinase inhibitor.

How Supplied

Caps—60, 90, 120

Generic Availability

NO

Gavreto Indications

Indications

Metastatic RET fusion-positive non-small cell lung cancer (NSCLC) as detected by an FDA approved test.

Gavreto Dosage and Administration

Adult

Confirm presence of a RET gene fusion. Take on an empty stomach. 400mg once daily. Continue until disease progression or until unacceptable toxicity. Concomitant use with combined P-gp and strong CYP3A inhibitors (if unavoidable): reduce to 200mg once daily if current dose is 300mg or 400mg once daily; reduce dose to 100mg once daily if current dose is 200mg once daily. Concomitant use with strong CYP3A inducers (if unavoidable): increase initial dose to double the current Gavreto dosage starting on Day 7 of concomitant use. Dose modifications for adverse reactions: see full labeling.

Children

Not established.

Gavreto Contraindications

Not Applicable

Gavreto Boxed Warnings

Not Applicable

Gavreto Warnings/Precautions

Warnings/Precautions

Monitor for pulmonary symptoms indicative of ILD/pneumonitis; withhold therapy and evaluate if occurs. Uncontrolled hypertension: do not initiate. Optimize BP prior to initiation; monitor after 1 week, then at least monthly thereafter and as clinically indicated. Hepatotoxicity. Monitor AST/ALT prior to initiation, every 2 weeks during 1st 3 months, then monthly thereafter and as clinically indicated. Permanently discontinue if severe or life-threatening hemorrhagic events occur. Risk of tumor lysis syndrome in those with MTC (esp. with rapidly growing tumors, high tumor burden, renal dysfunction, dehydration); monitor. Risk of impaired wound healing: withhold for ≥5 days prior to elective surgery; do not give for ≥2 weeks after major surgery and until adequate healing. Moderate (total bilirubin >1.5–3.0×ULN and any AST) or severe (total bilirubin >3.0×ULN and any AST) hepatic impairment. Embryo-fetal toxicity. Advise to use effective non-hormonal contraception during and for 2 weeks (females of reproductive potential) or 1 week (males w. female partners) after the last dose. Pregnancy: exclude status prior to initiation. Nursing mothers: not recommended (during and for 1 week after the last dose).

Gavreto Pharmacokinetics

See Literature

Gavreto Interactions

Interactions

See Adults. Potentiated by strong CYP3A inhibitors. Avoid concomitant combined P-gp and strong CYP3A inhibitors; if unavoidable, reduce Gavreto dose. Antagonized by strong CYP3A inducers; avoid concomitant use; if unavoidable, increase Gavreto dose. May antagonist hormonal contraceptives.

Gavreto Adverse Reactions

Adverse Reactions

Constipation, hypertension, fatigue, musculoskeletal pain, diarrhea; laboratory abnormalities (decreased lymphocytes, decreased neutrophils, decreased hemoglobin, decreased phosphate, decreased sodium, decreased calcium [corrected], increased ALT/AST/alkaline phosphatase, decreased platelets), pneumonia, pneumonitis, sepsis, UTI, pyrexia.

Gavreto Clinical Trials

See Literature

Gavreto Note

Not Applicable

Gavreto Patient Counseling

See Literature

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