Don’t let the high cost of brand specialty HER2-targeted antibody-drug conjugate stand between you and the treatment you need. We help eligible patients access Kadcyla (ado-trastuzumab emtansine) for as little as $69.95 per month through the manufacturer’s Patient Assistance Program
The Kadcyla Prescription Assistance Program is a manufacturer-sponsored initiative that provides Kadcyla infusions at little or no medication cost to qualifying patients based on income and insurance status. The program is designed for HER2+ breast cancer patients who are uninsured or underinsured, as well as Medicare beneficiaries.
Navigating the program on your own means dealing with eligibility verification, oncology-team coordination, HER2 testing documentation, prior-authorization documentation, infusion scheduling, cardiac monitoring schedules, and renewal deadlines.
AffordMyPrescriptions eliminates that burden. For a flat $69.95 per month, our Patient Advocates handle every step of your enrollment, from initial application through ongoing infusion-schedule coordination and annual re-certification — so you focus on your treatment, not paperwork.
| Pharmacy(With Coupon) | PrIce (30-Day)* | You Save W/ Us |
|---|---|---|
| Per IV infusion (typical) | ~$13,000.00 | Save ~$12,930/dose |
| Higher-weight patient | ~$15,000.00 | Save ~$14,930/dose |
| Per cycle (every 3 weeks) | ~$13,000+ | Save ~$12,930/cycle |
| Full 14-cycle adjuvant course | ~$180,000+ | Save ~$179,000+ total |
| Annual cost (metastatic) | ~$220,000+ | Save ~$219,000+/yr |
*Just a heads-up — retail prices are estimates based on public data and vary by pharmacy. AffordMyPrescriptions Advocacy Service bypasses this by using drug manufacturer programs to secure your medication directly at no cost or retail price.
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The Patient Assistance Program is free to apply for and provides Kadcyla infusions at little or no medication cost if approved. But the process involves detailed applications, oncology-team coordination, HER2 testing documentation, infusion scheduling, cardiac monitoring (echocardiograms or MUGA scans), and ongoing renewal management. Our $69.95/month service covers full advocacy.
Complete a simple eligibility form so our team can determine if you may qualify for medication assistance programs.
Our specialists help gather documentation, complete applications, and coordinate with program providers.
Once approved, you may receive your medication through the assistance program while we help manage ongoing paperwork and renewals.
Many patients try discount cards first. Here’s why the Patient Assistance Program through AffordMyPrescriptions is the better long-term solution for Kadcyla:
We manage all paperwork, refills, and annual renewals
Eligibility is generally determined by annual household income and insurance status. Most programs follow guidelines that include limits of up to $40,000 for individuals, $60,000 for couples, and $100,000 for larger families. Because requirements vary by program and household, we encourage you to contact AffordMyPrescriptions directly so we can review your specific situation and determine if you qualify for Kadcyla assistance.
Not sure if you qualify? Our pre-qualification check is completely free. If we can’t help, you won’t be charged.
Kadcyla (ado-trastuzumab emtansine, also known as T-DM1) is an intravenous (IV) HER2-targeted antibody-drug conjugate (ADC) used to treat HER2-positive breast cancer — both as adjuvant therapy after surgery in patients with residual disease following neoadjuvant therapy, and for HER2-positive metastatic breast cancer that has progressed on prior trastuzumab and a taxane.
How Kadcyla Works:
Kadcyla acts as a targeted chemotherapy delivery vehicle by combining the HER2-targeting antibody trastuzumab with a potent chemotherapy drug called DM1. The antibody portion attaches to HER2-positive cancer cells, allowing the entire molecule to enter the cell and release the chemotherapy directly inside. This specialized mechanism kills cancer cells from within while largely sparing healthy tissue, providing higher efficacy than traditional chemotherapy.
Form and use:
This medication is administered as an intravenous (IV) infusion every three weeks in a clinical or hospital setting. The weight-based dosage is typically given over 90 minutes for the first session and can be shortened to 30 minutes for subsequent doses if well-tolerated. For early breast cancer, treatment usually lasts for 14 cycles, while metastatic cases continue until the disease progresses or toxicity occurs.
Generic availability:
As of 2026, there is no FDA-approved biosimilar version of Kadcyla available in the United States. While other HER2-targeted antibody-drug conjugates like Enhertu have been approved for similar conditions, Kadcyla remains a unique branded therapy. The choice between these advanced treatments depends on a patient’s specific indication and prior treatment history as determined by an oncology team.
Warnings:
Kadcyla carries serious boxed warnings for liver injury, heart muscle weakness (cardiomyopathy), and embryo-fetal toxicity. Patients must undergo regular liver-function tests and cardiac monitoring before every treatment cycle to ensure safety. Other notable risks include lung inflammation, low platelet counts, and nerve damage; any symptoms like jaundice, bruising, or shortness of breath should be reported immediately.
Per-infusion costs commonly run $11,000–$15,000+ at the standard 3.6 mg/kg dose every 3 weeks. A full 14-cycle adjuvant course can total $150,000+. Through AffordMyPrescriptions, qualifying patients receive Kadcyla at no medication cost — our $69.95 monthly fee covers full advocacy and program management.
Both target HER2, but Kadcyla is an antibody-drug conjugate (ADC) — it combines trastuzumab (the antibody in Herceptin) with a potent chemotherapy molecule called DM1. Kadcyla delivers chemotherapy directly into HER2-expressing cancer cells, providing greater efficacy than Herceptin alone but with a different side-effect profile (including more thrombocytopenia and a higher risk of liver toxicity).
Like Herceptin, Kadcyla can cause cardiomyopathy (weakening of the heart muscle). Cardiac function (LVEF) is assessed at baseline and before each cycle with echocardiogram or MUGA scan. Most cases are reversible if caught early and treatment is paused or stopped.
There is no biosimilar to Kadcyla in the U.S. as of 2026. Other HER2-targeted ADCs (Enhertu/trastuzumab deruxtecan) are FDA-approved for some HER2-positive cancers — whether one is a better clinical fit depends on the indication, prior treatments, and tolerability. We mention this directly because if a different therapy on a more accessible assistance pathway would work, that may be a better path.
For early-stage breast cancer adjuvant therapy (after neoadjuvant treatment), Kadcyla is given for 14 cycles (approximately 9–10 months). For metastatic disease, treatment continues until progression or unacceptable toxicity.
If your initial application is denied, we explore alternatives — the manufacturer’s copay assistance program if you have commercial insurance, independent foundations such as the PAN Foundation, HealthWell Foundation, Susan G. Komen, or Living Beyond Breast Cancer, or asking your oncology team whether a different HER2-targeted therapy would be appropriate. If we cannot find a path, you will not be charged our service fee.
If you are struggling with the high cost of Kadcyla, our team may be able to help you access assistance programs designed to make brand specialty HER2-targeted ADC therapy affordable. Check your eligibility today.
Start free by filling out a simple online form.
Our specialist will contact you for a quick welcome call.
Our team handles everything, so you can focus on your health.