The VOWST Voyage™ program is here to support your patients
Financial assistance may be available for eligible patients
To get your patient started in the VOWST Voyage Patient Support program, you will need to complete and submit the VOWST® enrollment form and prescription either through the VOWST Voyage Prescriber Portal or print and fax.
Patients are not required to enroll in VOWST Voyage to access VOWST.
Case managers
Once enrolled, a case manager will get in touch with the patient to discuss program details.
Coverage and benefits investigation
We can help your patients:
Navigate insurance coverage and benefits
Investigate other options for coverage, including financial assistance programs that may help cover some of the out-of-pocket costs of VOWST for eligible patients
CO-PAY ASSISTANCE
Eligible commercially insured patients may pay as little as $0 for VOWST, with a maximum benefit of $9,100 per calendar year.*
*Offer not valid for patients whose prescriptions are reimbursed by Medicare, Medicaid, or other state or federal healthcare program, or where prohibited by law. To learn the full Terms, Conditions, and Eligibility requirements, visit VOWSTcopay.com.
VOWST PATIENT ASSISTANCE PROGRAM (PAP)
Uninsured or underinsured patients may be eligible to receive VOWST at no cost if they meet financial and other eligibility requirements.
VOWST VOUCHER PROGRAM
Eligible patients experiencing significant access issues related to insurance coverage may receive VOWST for free. Offer not valid where prohibited by law.
Welcome kit
Patients enrolled in VOWST Voyage may be eligible to receive a complementary welcome kit, which includes a laxative (magnesium citrate).
Over 92% of commercial and Medicare insured patients have access to VOWST with no step therapy requirements,† and over 90% of all first recurrent patients have been approved by payors nationally‡
†As of March 2024 and of published policies. Individual benefits may vary.
‡Data on file based on Specialty Pharmacy dispensing data from May 10, 2023 to May 22, 2024.1
ACCESS AND REIMBURSEMENT RESOURCES
Explore available financial and educational materials
VOWST is indicated to prevent the recurrence of Clostridioides difficile infection (CDI) in individuals 18 years of age and older following antibacterial treatment for recurrent CDI (rCDI).
Limitation of Use: VOWST is not indicated for treatment of CDI.
IMPORTANT SAFETY INFORMATION
WARNINGS AND PRECAUTIONS
Transmissible infectious agents: Because VOWST is manufactured from human fecal matter, it may carry a risk of transmitting infectious agents. Report any infection that is suspected to have been transmitted by VOWST to Aimmune Therapeutics, Inc. at 1-833-246-2566.
Potential presence of food allergens: VOWST may contain food allergens. The potential to cause adverse reactions due to food allergens is unknown.
ADVERSE REACTIONS
The most common adverse reactions (reported in ≥5% of Vowst-treated participants, and at a rate greater than placebo) were abdominal distension (31.1%), fatigue (22.2%), constipation (14.4%), chills (11.1%), and diarrhea (10.0%).
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Testing the category description for testing purposes
Multicenter, randomized, double-blind, placebo-controlled,
parallel-group trial in adults (≥18 years) with recurrent
C. diff1-3
Primary Endpoint
Recurrence at 8 weeks*
Secondary Endpoints
Adverse events within 24 weeks
Recurrence at 4, 12, 24 weeks*
Recurrence confirmed with C. diff toxin test and ≥3 unformed bowel movements per day over 2 days*
10–21 days of vancomycin (125 mg QID) or fidaxomicin (200 mg BID)
ECOSPOR III efficacy endpoints based on intent-to-treat population.
Data were rounded to the nearest whole number for presentation.
STUDY DESIGN
ECOSPOR IV was an open-label, single arm study
of 263 participants with ≥1
C. diff
recurrences
evaluating the safety of VOWST;
the secondary endpoint was efficacy5
Limitations: open-label study design yields descriptive results limiting interpretations of efficacy and safety without a comparator
ECOSPOR IV
Multicenter, open-label, single-arm trial
in adults (≥18 years) with recurrent
C. diff5
Primary Endpoint
Adverse events within 24 weeks
Secondary Endpoints
Recurrence at 4, 8, 12, 24 weeks
Recurrence confirmed with
C. diff
toxin test
or
PCR
and ≥3 unformed bowel movements per day over 2 days*
10–42 days of vancomycin
or 10–25 days of fidaxomicin
Toxin and PCR testing were utilized to determine initial eligibility. Recurrences while on study were confirmed by toxin testing to ensure study integrity.
†25 placebo recipients and 4 VOWST recipients discontinued ECOSPOR III and enrolled in ECOSPOR IV after experiencing a C. Diff recurrence within 8 weeks.
Data were rounded to the nearest whole number for presentation.