Relapsing polychondritis

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3Active trials9Specialists8Treatment centers

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Overview

Relapsing polychondritis (sometimes called RP or systemic chondromalacia) is a rare autoimmune disease in which the body's immune system mistakenly attacks cartilage — the firm but flexible tissue that gives shape and structure to your ears, nose, throat, windpipe, and joints. The disease tends to come and go in episodes called 'flares,' which is where the word 'relapsing' comes from. During a flare, affected cartilage becomes red, swollen, and painful, and over time it can break down and lose its shape. Relapsing polychondritis can affect many parts of the body. The ears and nose are most commonly involved, often becoming red and tender during flares. The airways — including the voice box and windpipe — can also be affected, which is one of the most serious aspects of the disease. The eyes, heart, blood vessels, kidneys, and skin may also be involved in some people. Treatment focuses on calming the immune system and reducing inflammation. Mild cases may be managed with anti-inflammatory medicines like NSAIDs or dapsone. More severe cases often require corticosteroids (such as prednisone) or stronger immune-suppressing drugs. Newer biologic therapies are being explored. There is currently no cure, but many people can manage their symptoms and live active lives with the right treatment plan.

Also known as:

Key symptoms:

Red, swollen, and painful outer ears (but not the earlobes, which have no cartilage)Saddle-nose deformity — the bridge of the nose collapses over timeJoint pain and swelling in multiple jointsHoarse voice or difficulty speakingShortness of breath or noisy breathing due to airway narrowingEye redness, pain, or vision changesHearing loss or ringing in the earsDizziness or balance problemsSkin rashes or nodulesChest pain or tenderness over the breastboneFatigue and general feeling of being unwellHeart valve problems in some casesKidney problems in some cases

Clinical phenotype terms (50)— hover any for plain English
Large vessel vasculitisHP:0005310ChondritisHP:0100662Chondritis of pinnaHP:0200047Abnormal aortic valve morphologyHP:0001646TracheobronchomalaciaHP:0002786AtelectasisHP:0100750
Inheritance

Sporadic

Usually appears on its own, not inherited from a parent

Age of Onset

Adult

Begins in adulthood (age 18 or older)

Orphanet ↗NORD ↗

FDA & Trial Timeline

3 events
Aug 2025An Open-Label Study of Effectiveness of Immunomodulatory Medications for Patients With Relapsing Polychondritis

University of Pennsylvania — PHASE2

TrialRECRUITING
Nov 2024Efficacy, Safety and Immunological Evaluation of Upadacitinib for Relapsing Polychondritis

Peking University People's Hospital — PHASE1, PHASE2

TrialRECRUITING
Feb 2021Longitudinal Study for Relapsing Polychondritis

University of Pennsylvania

TrialRECRUITING

Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Treatments

No FDA-approved treatments are currently listed for Relapsing polychondritis.

3 clinical trialsare actively recruiting — trials can provide access to cutting-edge therapies.

View clinical trials →

Clinical Trials

3 recruitingView all trials with filters →
Phase 21 trial
An Open-Label Study of Effectiveness of Immunomodulatory Medications for Patients With Relapsing Polychondritis
Phase 2
Actively Recruiting
PI: Shubhasree Banerjee, MD (University of Pennsylvania) · Sites: Philadelphia, Pennsylvania · Age: 1899 yrs
Other1 trial
Longitudinal Study for Relapsing Polychondritis
Actively Recruiting
PI: Peter Merkel, MD, MPH (University of Pennsylvania) · Sites: Philadelphia, Pennsylvania

Specialists

9 foundView all specialists →
ZL
Zhanguo Li
Specialist
PI on 7 active trials819 Relapsing polychondritis publications
SP
Samuel K Shinjo, PhD
Specialist
PI on 3 active trials
SM
Shubhasree Banerjee, MD
PHILADELPHIA, PA
Specialist
PI on 2 active trials
LZ
Li Zhanguo
Specialist
PI on 1 active trial
PM
Peter C Grayson, M.D.
BOSTON, MA
Specialist
PI on 2 active trials
ML
Maggie Larché
Specialist
PI on 1 active trial
AZ
Ariane ZALOSZYC
Specialist
PI on 1 active trial

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Relapsing polychondritis.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Relapsing polychondritis

Disease timeline:

New recruiting trial: Longitudinal Study for Relapsing Polychondritis

A new clinical trial is recruiting patients for Relapsing polychondritis

New recruiting trial: Efficacy, Safety and Immunological Evaluation of Upadacitinib for Relapsing Polychondritis

A new clinical trial is recruiting patients for Relapsing polychondritis

New recruiting trial: An Open-Label Study of Effectiveness of Immunomodulatory Medications for Patients With Relapsing Polychondritis

A new clinical trial is recruiting patients for Relapsing polychondritis

Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Questions for your doctor

Bring these to your next appointment

  • Q1.How do I know if my symptoms are a flare, and when should I go to the emergency room?,Which organs are currently affected in my case, and how will you monitor them over time?,What are the risks and benefits of long-term corticosteroid use, and is there a plan to reduce my dose?,Are there clinical trials or newer biologic treatments I might be eligible for?,How often should I have breathing tests or imaging to check my airway?,Should I see other specialists such as a pulmonologist, cardiologist, or ENT doctor?,What signs should prompt me to seek emergency care immediately?

Common questions about Relapsing polychondritis

What is Relapsing polychondritis?

Relapsing polychondritis (sometimes called RP or systemic chondromalacia) is a rare autoimmune disease in which the body's immune system mistakenly attacks cartilage — the firm but flexible tissue that gives shape and structure to your ears, nose, throat, windpipe, and joints. The disease tends to come and go in episodes called 'flares,' which is where the word 'relapsing' comes from. During a flare, affected cartilage becomes red, swollen, and painful, and over time it can break down and lose its shape. Relapsing polychondritis can affect many parts of the body. The ears and nose are most co

How is Relapsing polychondritis inherited?

Relapsing polychondritis follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Relapsing polychondritis typically begin?

Typical onset of Relapsing polychondritis is adult. Age of onset can vary across affected individuals.

Are there clinical trials for Relapsing polychondritis?

Yes — 3 recruiting clinical trials are currently listed for Relapsing polychondritis on UniteRare. See the clinical trials section on this page for phase, sponsor, and site details sourced from ClinicalTrials.gov.

Which specialists treat Relapsing polychondritis?

9 specialists and care centers treating Relapsing polychondritis are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.