Short answer · Medically reviewed summary · Last updated: 2026-05-08

Currently, there is no medical cure for Relapsing Polychondritis, a rare autoimmune condition characterized by recurrent inflammation of cartilage. While a cure does not exist, modern medical management focused on early intervention and targeted immunosuppression can effectively induce remission, manage symptoms, and prevent permanent structural damage to the airway and joints. How is Relapsing Polychondritis managed today? Treatment for Relapsing Polychondritis centers on controlling systemic inflammation to preserve cartilage integrity.

12 people with Relapsing Polychondritis have shared their first-person experience on this question at DiseaseMaps.

13

Does Relapsing Polychondritis have a cure?

Is there a cure for Relapsing Polychondritis? Current treatment landscape and research progress, medically reviewed, plus patient experiences.

Relapsing Polychondritis cure

Currently, there is no medical cure for Relapsing Polychondritis, a rare autoimmune condition characterized by recurrent inflammation of cartilage. While a cure does not exist, modern medical management focused on early intervention and targeted immunosuppression can effectively induce remission, manage symptoms, and prevent permanent structural damage to the airway and joints.



How is Relapsing Polychondritis managed today?


Treatment for Relapsing Polychondritis centers on controlling systemic inflammation to preserve cartilage integrity. Physicians typically employ a stepwise approach, starting with corticosteroids like prednisone to address acute flares. For patients with persistent disease, clinicians may introduce disease-modifying antirheumatic drugs (DMARDs) or biologic agents to maintain remission and reduce the long-term reliance on steroids.



What research is being done to find a cure?


Research into Relapsing Polychondritis is evolving rapidly as our understanding of its underlying immunological drivers improves. Scientists are currently investigating the following areas:



  • Biologic Therapies: Clinical studies are evaluating the efficacy of targeted therapies, such as TNF-alpha inhibitors and IL-6 inhibitors, to block specific inflammatory pathways.

  • Precision Medicine: Researchers are working to identify specific biomarkers that can predict disease flares or help tailor drug selection to the individual’s immune profile.

  • Immunomodulation: Investigations into the role of B-cell depletion therapies are providing new insights into how to potentially "reset" the immune response in Relapsing Polychondritis patients.



Can patients participate in clinical trials?


Yes, participation in clinical research is vital for advancing care for Relapsing Polychondritis. Because this is a rare disease, international collaboration is essential to gather enough data for significant breakthroughs. Patients are encouraged to monitor registries and trial databases to identify studies that match their specific clinical history.



Next steps



  • Consult with a rheumatologist who specializes in systemic autoimmune or vasculitic conditions.

  • Join the Relapsing Polychondritis community at DiseaseMaps.org to connect with 468 other members sharing experiences and trial updates.

  • Regularly check ClinicalTrials.gov for newly opened studies relevant to relapsing autoimmune disorders.



Medical disclaimer: This information is for educational purposes only and does not replace professional medical advice, diagnosis, or treatment.



References



  • NIH Genetic and Rare Diseases Information Center (GARD): Relapsing Polychondritis

  • Orphanet: Rare Disease Database (ORPHA:732)

  • OMIM (Online Mendelian Inheritance in Man): Relapsing Polychondritis entry

  • Relapsing Polychondritis Foundation: Patient Resources and Research Updates

Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2026-05-08
Medical disclaimer: This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source: DiseaseMaps.org
13 answers
There is no cure for Relapsing Polychondritis. No active work/research is being done to find a cure. We have to hope that a cure for another Autoimmune Disease will work for us.

Posted Aug 9, 2017 by Louise C 1450
No, not that I am aware of.

Posted Aug 14, 2017 by Susan 2000
No cure that I know of. Only temporary fixes. I don't think we are going to find a cure anytime soon. There is not enough money for research due to the fact that so few people have this disease.

Posted Sep 1, 2017 by Diane 2050
no.. however, by the nature of Relapsing Polychondritis..the symptoms can come and go..

Posted Mar 20, 2018 by Lisa Matthews (Lissy) 4800
Unfortunately not yet

Posted Jun 12, 2019 by Laoura 2050
No its incurable at this time

Posted Jun 12, 2019 by Tmrcarlson 3550
There is no cure for relapsing polychondritis.

Posted Jun 12, 2019 by Kaz 3000
There is no cure, but with the right treatment to stop flares, the disease can be slowed down

Posted Dec 30, 2019 by Leanne 2500
As yet no, no cure has been found

Posted Dec 30, 2019 by Carrie 3050
No, I don't think so. Progress has been made in the treatment of the symptoms.

Posted Mar 20, 2022 by shlawver 2500
Translated from spanish Improve translation
Doctors say that , not

Posted Oct 2, 2017 by Ana Luiza Bottura 2000
Translated from spanish Improve translation
I don't know, is a disease autoinmunologica

Posted Oct 2, 2017 by Kevin Ochoa 2000

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Stories of Relapsing Polychondritis

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Relapsing Polychondritis stories
The first time I noticed symptoms, I thought I was having an allergic reaction to something at work. My ears became so red and inflamed and hurt so bad. I let it go on for almost 3 days before finally going to a hospital where I was diagnosed with re...
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It began with dry nose, nose bleeding and what my GP thought was a sinus infection. Antibiotics and prednisone perscribed, helped for a while, then reoccurred. Ear then swelled over twice the size - red, shiny and moist, GP again said outer ear infec...
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i had progressively worsening breathing issues for many years before my diagnosis of rp.  I went through many specialists and tests and no one could identify why I was having breathing issues.  I had no outward signs of rp until one day my ears swe...
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I was officially diagnosed with RP 2 yrs ago. No one else in my family has it. It started approximately 5 years ago with ear flares, jumping from one to the other. My PCP happened to go to a conference where RP was discussed, and soon contacted me to...
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I have had strange symptoms before this came to light, but during my last trimester of my pregnancy with my youngest son, I had a severe respiratory infection that never seemed to get better. I have had exercise induced asthma since I was young and t...

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Relapsing Polychondritis forum

RELAPSING POLYCHONDRITIS FORUM
Relapsing Polychondritis forum
I don't think RP is as rare as we are led to believe. It seems many symptoms are unrelated. You go to an ortho doc for knee/joint pain. You go to an ENT for ears and throat. You go to an ophthalmologist for eyes. You go to a dermatologist for skin. T...

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