Explore every approved treatment, every open clinical trial, and every option your doctor might not know to mention — all in plain English, all in one place. Browse anonymously. No account required.
You're likely here because you — or someone you love — has just been diagnosed with cancer. Maybe you've already spent hours searching the internet and found nothing but statistics that terrified you, medical jargon written for doctors, and information that left you more confused than when you started.
Your Cancer Path was built specifically for this moment. Every approved treatment, every open clinical trial, every promising drug in development — explained in plain English, sourced from the FDA and peer-reviewed research, and presented without judgment or agenda. No miracle cures. No hype. Just facts.
This is not a substitute for your oncologist. But it will help you walk into that office better informed, with better questions, and a clearer picture of every path available to you. That's all we're trying to do.
Select a cancer type below to explore every approved treatment, open clinical trial, and promising investigational drug — in plain English.
Browse every cancer type above, or use the Explore page to find treatments, open trials, and promising drugs for any diagnosis.
Every treatment, side effect, and efficacy rate is sourced from FDA approvals, peer-reviewed studies, and ClinicalTrials.gov. We cite everything. This site is primarily U.S.-focused — international visitors should verify approval status with their local regulatory authority.
Browse everything without creating an account. No email required. No tracking. Your health search is your business alone.
Every open, enrolling clinical trial pulled directly from ClinicalTrials.gov — filtered, simplified, and explained in plain English.
Our community is moderated by cancer survivors who've been through it. Every post is reviewed before publishing. Real experiences, verified.
These are drugs that have shown meaningful results in clinical trials but have not yet received full FDA approval. They may be available through clinical trial enrollment, compassionate use, or Right to Try. All data is factual and sourced from published trial results.
Care pathways show the typical sequence of treatment decisions — from first-line options through salvage and escalation if earlier treatments stop working. These reflect how oncologists generally think about sequencing, not a prescription for any individual patient. Always discuss your specific situation with your care team.
Select a cancer type to explore every approved treatment, open clinical trial, and promising investigational drug.
Live data pulled from ClinicalTrials.gov. Every trial listed is actively recruiting. Search by cancer type or keyword below.
Most patients who qualify never find out about trials they're eligible for. Your Cancer Path was built to change that. Reading this page is the first step.
Enter your city to find actively enrolling trials within your area. Optionally filter by cancer type, drug name, or company. Results pull directly from ClinicalTrials.gov and include contact information for each site.
The Right to Try Act (2018) and the FDA's Expanded Access program give seriously ill patients legal pathways to access investigational drugs. Here's exactly how to pursue them.
This guide is for informational and educational purposes only. It is not legal or medical advice. Your Cancer Path strongly recommends consulting with your oncologist and, where appropriate, a healthcare attorney before pursuing any of these pathways. Laws vary by state and situation.
The Right to Try Act and FDA Expanded Access programs described on this page are U.S.-specific legal pathways. If you are outside the United States, similar programs may exist in your country under different names and rules. For example, Health Canada administers the Special Access Program (SAP) for unapproved drugs. The European Medicines Agency (EMA) and individual EU member states have their own compassionate use frameworks. Australia's TGA offers the Special Access Scheme. The approval status, eligible indications, and available warnings for any given drug may also differ from what the FDA has approved. Please speak with an oncologist or specialist in your country who can advise on what pathways are available to you locally.
Under the Right to Try Act, you must: (a) have a life-threatening diagnosis confirmed by a licensed physician; (b) have tried all approved treatment options or be unable to participate in a clinical trial; (c) be unable to participate in a clinical trial for the drug you're seeking. Your physician must certify all of this in writing.
Under Right to Try, the request goes directly to the drug manufacturer — not to the FDA. You do not need FDA approval for this pathway. Search ClinicalTrials.gov for the drug sponsor's contact information. Many biotech companies have a "Compassionate Use" or "Medical Affairs" department specifically for these requests.
The manufacturer will require a letter from your treating physician confirming your diagnosis, treatment history, and why they support this request. Your doctor must also agree to monitor your treatment and report outcomes. Here is a script you can use to ask your doctor to write this letter.
Manufacturers are not required to provide the drug — they can say no. But many will say yes, especially if you're a good candidate who adds to their safety data. Insurance typically does not cover Right to Try drugs. Ask the manufacturer about patient assistance programs or compassionate pricing. Some patient advocacy groups can help fund this.
Expanded Access involves the FDA directly. The FDA approves approximately 99% of Expanded Access requests, and the average review time for emergency requests is just 24 hours. For non-emergency requests, it is typically a few days to weeks. This pathway has more oversight but also more support.
Your treating physician submits an Expanded Access request directly to the FDA. This is the form that allows an individual patient to access an unapproved drug. The FDA's Oncology Center of Excellence has a dedicated helpline: 1-855-5-CANCER (1-855-522-6237). Show your doctor this page and ask them to contact the FDA directly.
Just like Right to Try, the drug manufacturer must agree to provide the drug. The FDA can approve the request but cannot force a company to provide its drug. Contact the manufacturer's Medical Affairs department in parallel with the FDA process.
FDA Office of Oncology Products: [email protected]
FDA Expanded Access Navigator: expandedaccess.fda.gov
Patient Advocate Foundation: 1-800-532-5274
National Organization for Rare Disorders (NORD): 1-800-999-6673
Many doctors are unfamiliar with Right to Try or Expanded Access. Some may be hesitant. Here is language you can use:
"I've been researching [drug name] and I understand it's currently in Phase [X] trials with promising results for my diagnosis. I'd like to explore whether I might be a candidate for Right to Try or FDA Expanded Access. Would you be willing to look into submitting a request on my behalf? I can bring you the FDA Form 3926 and the manufacturer's contact information. This is important to me and I'd like your partnership in exploring it."
Share your journey. Read others. Ask questions. Every post is reviewed by a volunteer moderator — a cancer survivor — before it goes live. You are not alone.
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Your Cancer Path is a research, education, and peer support platform for cancer patients, survivors, caregivers, and their families. It is not a medical practice, does not provide medical advice, and is not a substitute for consultation with a licensed physician or oncologist.
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"I've had my own experience with cancer. Years ago I faced a diagnosis that shook my world and opened my eyes to how hard it is to navigate the medical system when you're scared and don't know what questions to ask. I survived. I consider myself one of the lucky ones. But it was losing a close friend to cancer this past November that became the real catalyst behind Your Cancer Path."
He was someone I genuinely liked and admired — we first crossed paths in the 1990s, and when I found out about his diagnosis, something in me just couldn't stand by. I was determined to help him find every option available — not just the standard path, but everything. Clinical trials. Experimental drugs. Expanded Access. Right to Try. I believed then, and I believe now, that there were options worth exploring that might have given him more time.
What I found instead was a wall — not built by any one person, but by a system with layers of complexity that most patients and families have no idea exist.
He went through chemotherapy. He tried a targeted radiation therapy that made him miserable — the side effects were severe, and there were stretches where he was essentially confined to home because of how his body responded. He lost feeling in his feet. He was exhausted and in pain. And through all of it, he kept fighting.
I worked closely with him and his wife. I went to doctor's appointments with them. I tried to help navigate a path toward an investigational drug — one the manufacturer was willing and ready to provide. The drug company said yes. There was no guarantee it would have worked. But we wanted the chance to try.
What we ran into was the reality of how complex these pathways are. The paperwork. The liability concerns. The way our medical system is structured around standard of care — for reasons that aren't always wrong, but that can leave patients without options when time is short. His physician had real concerns, including around malpractice coverage, and I came to understand that those concerns are part of a bigger, broken system — not a reflection of any one doctor's heart. But in the moment, it felt like a door closing.
His wife didn't know these pathways existed. My friend didn't know. Most people don't — because nobody tells them. I reached out to physicians across the country trying to find someone who could help us move forward. A few pointed us in directions that required steps we couldn't complete in time.
My friend fought with everything he had. In the end, the cancer spread to his brain, his lungs, his entire body. He passed away in November. He is out of pain now. But I carry the weight of knowing that information and access existed that he never got to — and that we just couldn't connect him to it in time.
Your Cancer Path exists because of him. It exists for the patient who was just diagnosed and doesn't yet know what the road ahead might look like — what the diagnostic process involves, what questions to ask, and what options exist before treatment even begins. It exists for the patient already in treatment who wonders whether there is something else worth trying. It exists so that every patient — and their spouse, and their family — walks into every appointment knowing every option on the table. So they know what a clinical trial is and how to find one. So they know what Expanded Access means and how to start that conversation with their doctor. So they know that if one door closes, there may be others worth knocking on. I am not a doctor. This platform is not medical advice. But it is here, and it is free, and no one should have to navigate this alone.
To put factual, comprehensive, plain-English cancer treatment information in the hands of every patient and family who needs it — free, anonymous, and without agenda — so they can have better conversations with their doctors and find the right path faster.
Your Cancer Path is independently operated. Pharma sponsors pay to reach our opted-in community — they do not pay to shape what we publish. Every fact is cited. Every source is disclosed. Our medical advisory board reviews all clinical content independently.
Your Cancer Path operates as two connected entities: Your Cancer Path Inc. (the tech company that builds and maintains the platform) and Your Cancer Path Foundation (the nonprofit that funds free access for patients who can't afford anything). Founding Memberships and Build Faster contributions go to the tech company. Fund a Fighter donations go directly to the nonprofit foundation. Full financial transparency is published quarterly.
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Your Cancer Path is currently in beta. Whether you're a patient, caregiver, medical professional, or potential partner — we'd love to stay in touch as we build toward full launch.
The content on Your Cancer Path has not yet been reviewed by a licensed medical professional. All information is sourced from the FDA, ClinicalTrials.gov, and peer-reviewed publications, but please treat this as a starting point for conversations with your oncologist — not a substitute for professional medical advice.
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