Ramantamig clinical trials
Ramantamig is named as an intervention in 9 current clinical trials in our USA, Spain, France, Netherlands, Australia, Israel, UK, Japan, Germany, Italy, South Korea, China, Brazil, Poland, Turkey, Canada, Portugal, Czechia, Belgium, Norway, Sweden, Egypt, India and Taiwan registers. 8 are recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Janssen Research & Development, LLC (8). The most-studied condition is Multiple Myeloma.
Patient leaflets for Ramantamig
The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.
- UKUnited Kingdom: Search MHRA ProductsPatient information leaflets and SmPCs for UK-licensed products.
- USUnited States: Search DailyMedFDA-approved labels, including patient and medication guides.
Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.
Trials by status
Trials by phase
Clinical trials of Ramantamig
9 trialsRegisters list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.
Conditions studied with Ramantamig
5 conditionsSponsors
lead sponsor per trial| Lead sponsor | Trials |
|---|---|
| Janssen Research & Development, LLC | 8 |
| University of Heidelberg Medical Center | 1 |
By country register
A trial with sites in more than one country appears in each of those registers.
Related compounds
Questions about Ramantamig trials
How many clinical trials are testing Ramantamig?
9 current trials in our USA, Spain, France, Netherlands, Australia, Israel, UK, Japan, Germany, Italy, South Korea, China, Brazil, Poland, Turkey, Canada, Portugal, Czechia, Belgium, Norway, Sweden, Egypt, India and Taiwan registers name Ramantamig (also registered as JNJ-79635322) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.
Are Ramantamig trials recruiting patients?
Yes. 8 of the 9 trials are recruiting: 6 with sites in USA, 7 with sites in Spain, 5 with sites in France, 5 with sites in Netherlands, 5 with sites in Australia, 4 with sites in Israel, 4 with sites in UK, 3 with sites in Japan, 4 with sites in Germany, 3 with sites in Italy, 3 with sites in South Korea, 2 with sites in China, 3 with sites in Brazil, 2 with sites in Poland, 2 with sites in Turkey, 2 with sites in Canada, 2 with sites in Portugal, 2 with sites in Czechia, 1 with sites in Belgium, 1 with sites in Norway, 1 with sites in Sweden, 1 with sites in Egypt, 1 with sites in India and 1 with sites in Taiwan. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
Who sponsors Ramantamig clinical trials?
Janssen Research & Development, LLC (8) and University of Heidelberg Medical Center (1). The number in brackets is how many trials each organisation leads.
Where does this information come from?
Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Ramantamig works or whether it is effective, and it is not medical advice.
How this page is built
Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Ramantamig works or whether it is effective. Each trial links to its own record so you can check it yourself.
- ClinicalTrials.gov (U.S. National Library of Medicine) ↗ Trial IDs, titles, intervention names and synonyms, phase, overall status, lead sponsor and conditions for every trial on this page
This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Ramantamig (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.