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2024 Guide to Patient Support Services

Exelixis

2024 PSS Guide

Exelixis Access Services

Exelixis Access Services (EASE) includes programs designed to support patients who are prescribed Exelixis oncology drugs Cabometyx or Cometriq (Table).

EASE Programs

The EASE programs are drug-specific and provide financial, access, and reimbursement support for eligible patients.

To enroll your patients who have been prescribed Cabometyx, visit Ease.us. To enroll your patients who have been prescribed Cometriq, visit www.cometriq.com/hcp/access.

Cabometyx 30-Day Free Trial Program

The 30-Day Free Trial Program provides a free trial to help new Cabometyx patients start treatment quickly, regardless of insurance type. A 30-day additional supply may be available to patients with a payer decision delay of ≥5 days. Restrictions and eligibility rules apply.

EASE Dose Exchange Program

The Dose Exchange program provides a free 15-tablet supply of Cabometyx in the lower dose to help patients who require a dose reduction. restrictions and eligibility rules apply.

EASE Co-Pay Program

Eligible patients with commercial insurance will pay $0 per month for Cabometyx or Cometriq. eligibility restrictions apply.

EASE Patient Assistance Program

Eligible patients who are uninsured or are insured but cannot afford the cost of the medication may receive Cabometyx or Cometriq free of charge.

TABLE Exelixis Oncology Drugs

Drugs
Indications
Patient support programs


Drug
Cometriq (cabozantinib) capsules
Indications
Treatment of progressive, metastatic medullary thyroid cancer
Patient support programs

Cabometyx (cabozantinib) tablets Indications

Treatment of patients with advanced renal-cell carcinoma (RCC); first-line treatment of patients with advanced RCC in combination with nivolumab; treatment of patients with hepatocellular carcinoma who have been previously treated with sorafenib; treatment of adult and pediatric patients aged ≥12 years with locally advanced or metastatic differentiated thyroid cancer that has progressed following prior vascular endothelial growth factor receptor–targeted therapy and who are radioactive iodine-refractory or ineligible