New hope for immunotherapy side effects: blood filtering may replace steroids
NCT ID NCT07619898
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a treatment called extracorporeal photopheresis (ECP) for people with advanced melanoma who develop severe colitis or hepatitis from immunotherapy. ECP filters a patient's blood, treats it with a light-activated drug, and returns it to the body. The trial compares ECP to standard second-line drugs like infliximab or vedolizumab. About 112 participants will be enrolled to see if ECP can help them stop steroids and control the side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- extracorporeal photopheresis (ECP) with methoxsalen
- What this could lead to
- If successful, ECP could offer a new steroid-free option for managing severe gut or liver side effects from melanoma immunotherapy.
- What could go wrong
- This is a phase 2 trial with only 112 participants, so results are preliminary. ECP is a complex blood-filtering procedure and may not work better than existing drugs.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
About 112 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Jul 2026
An estimate. Start dates often move.
- Expected to finish
-
Dec 2029
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Participants diagnosed with unresectable or metastatic melanoma ( Stage III and Stage IV) received ICI treatment (e.g., anti-PD-1, anti-PD-L1, anti-LAG-3, anti-CTLA-4 antibody, as ICI monotherapy or ICI combination therapy) and ICI paused or discontinued because of the development of ir-colitis or ir-hepatitis. 2. Participants diagnosed with ir-colitis and/or ir-hepatitis with a severity of Grade 2 or higher, based on ASCO Guidelines ( 3. Participants with endoscopic evidence of ir-colitis 4. Participants with inadequate response to corticosteroids, as defined per protocol 5. Participants who have Eastern Cooperative Oncology Group (ECOG) performance status 0, 1 or 2. Exclusion Criteria: 1. Presence of irAEs in addition to and other than ir-colitis and/or ir-hepatitis, with a higher severity grade than the irAE for inclusion (ir-colitis/ir-hepatitis) based on ASCO guidelines. 2. Participant has a diagnosis of uveal melanoma as the sole melanoma subtype 3. Treatment of ir-colitis or ir-hepatitis with any systemic therapy other than corticosteroids 4. Concurrent conditions which may require treatment with high dose corticosteroid (\> 1 milligram per kilogram per day \[mg/kg/day\]) and interfere with the corticosteroid tapering schedule recommended by the protocol. 5. Pre-existing liver disease 6. Active alcohol use disorder 7. Concomitant treatment with any chemotherapy or targeted therapy for the treatment of unresectable or metastatic melanoma. 8. Use of any investigational agent within 5 half-lives of the investigational agent prior to randomization. 9. Contraindications or known allergic reaction to any of study intervention and/or procedures 10. Participants unable to tolerate the fluid shift associated with the ECP procedure. 11. Positive result for active or previous viral infections: covid-19, hepatitis B/C, CMV, EBV, adenovirus 12. History of previous or concurrent malignancies within the last 3 years, other than unresectable or metastatic melanoma.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Colitis are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The study's own enquiry address
This study publishes an address for enquiries. See it below .
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Study contacts
-
Contact
Email: •••••@•••••
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a Two-Drug combo outsmart advanced melanoma?
- Your gut bacteria may hold the key to whether immunotherapy works
- Can a DNA vaccine teach the immune system to hunt melanoma?
- Can protein patterns in stored tumors point to new treatment targets?
- Can a Two-Drug immune combo shrink melanoma tumors?
- Can a Gut-Targeting drug shield cancer patients from Immunotherapy's worst side effect?