Ichthyosis Bullosa of Siemens clinical trials
The registry lists 24 studies for Ichthyosis Bullosa of Siemens across more than 10 countries. 6 are recruiting or about to start. 7 of them are mainly about Ichthyosis Bullosa of Siemens (how this is decided). Per ClinicalTrials.gov, last updated 2026-10-28.
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Who runs them
Mayo Clinic (3) · Oy Karl Fazer Ab (2) · University of North Carolina, Chapel Hill (2) · Biocodex (1) · Universitas Indonesia (1) · University of Auckland, New Zealand (1) · Karolinska Institutet (1) · Zagazig University (1)
Who develops what
Add to watchlistEvery program with a company-led study here in the last two years, whatever its size: 1 program from 1 company, 0 with this as their studies’ main aim; 1 with a live phase 3 study; 0 primary completions in the next 12 months.
Comparator & background therapies
What other companies’ phase 2+ studies give as the comparator or the background here (its leading trial sponsor and partners left out): a sign of what new drugs are measured against, not by itself the standard of care, its prescriptions or its market.
None given by two companies or more yet.
Programs
“Meets, by arms” reads each study’s arms: vs its arm against the therapy’s; + X vs a combination against it; added to it plus the therapy against the therapy; studied with given together only. The next primary completion is the next phase-3 study’s when there is one.
The 1 program — sign in to see the whole list, free: filter by phase and aim, sort by late development, direct comparisons or the next primary completion.
Primary completion in the next 12 months (0)
Live phase 2 and 3 studies of these programs. Primary completion is when the main measure’s data collection ends, as the registry states it (most are estimates); results come later, if they are announced.
None in the next 12 months.
Read from ClinicalTrials.gov, industry-led studies. Main aim: this is the study’s judged main condition; named, not the main aim: the sponsor names it, the study is about something else; registry mapping only: only the registry’s mapping put it here. Leading trial sponsor is the company leading the most industry studies of a drug, a measure of trial activity, not of rights. US and EU rights, and Approved: from the regulators’ records (FDA’s Drugs@FDA via openFDA; EMA’s medicines data) — the holder of a marketed or authorized original, generics and other companies’ versions; not rights elsewhere, nor approval for this condition. Phase 4 trial recorded, where neither lists it: a phase 4 study exists somewhere. Not read yet: labels by indication, exclusivity, licenses, line of therapy, academic comparators, sales.
What is being tested here
Drugs under test in Ichthyosis Bullosa of Siemens studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
| Drug | Open | Phase 3 | All |
|---|---|---|---|
| Saccharomyces cerevisiae | 1 | 1 | 1 |
| Rimegepant | 0 | 0 | 1 |
| Curcumin | 0 | 0 | 1 |
| Chenodeoxycholic Acid | 0 | 0 | 1 |
Coming up
Studies recruiting or running, from their records. “Main data collection” ends at the primary completion date, the sponsor’s own estimate, which often moves.
All 2
- Jan 2027Co-Development and Validation of Colonic Symptom Pictograms for Young People · University of Auckland, New Zealand
- Nov 2027Transcutaneous Electrical Acustimulation for IBS-D: A Multicenter Study · First People's Hospital of Foshan
Who these studies take
Of the 2 Ichthyosis Bullosa of Siemens studies recruiting now, 0 (0%) set no upper age limit and 2 (100%) stop at 75 or younger. 0 (0%) take children under 18. 0 (0%) are for women only and 0 (0%) for men only; 0 (0%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 0 (0%) | 0 (0%) |
| 18 | 2 (100%) | 2 (100%) |
| 30 | 2 (100%) | 2 (100%) |
| 40 | 2 (100%) | 2 (100%) |
| 50 | 2 (100%) | 2 (100%) |
| 65 | 2 (100%) | 2 (100%) |
| 75 | 0 (0%) | 0 (0%) |
| 85 | 0 (0%) | 0 (0%) |
Across all 24 studies, recruiting or not: 92% stop at 75 or younger and 67% at 65; 21% take children; 13% are for women only and 0% for men only; 21% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
What changed recently
From the registry's own updates since Oct 16, 2026.
Newly registered1
Studies
Recruiting first, then most recently updated. Showing 24 of 24. search them.
- Acupuncture Combined With Transcutaneous Electrical Acupoint Stimulation for Constipation-Predominant Irritable Bowel Syndrome With Anxiety StateNot yet recruitingNCT07899944Not applicable
- Phase III Clinical Trial of Changji'an Capsules in the Treatment of Irritable Bowel Syndrome With Predominant Diarrhea (Liver-Qi Invading Spleen Syndrome)Not yet recruitingNCT07610434Phase 31 country
- Transcutaneous Electrical Acustimulation for IBS-D: A Multicenter StudyNot yet recruitingNCT07425145Not applicable1 country
- Co-Development and Validation of Colonic Symptom Pictograms for Young PeopleNot yet recruitingNCT07337343
- Saccharomyces Boulardii CNCM I-745 in Irritable Bowel SyndromeRecruitingNCT07168434Phase 32 countries
- The Beneficial Effects on the Intestinal Function of a Food Supplement Based on an Extract of Green Tea and a Pool of Probiotics in Subjects With Irritable Bowel Syndrome With Predominance of ConstipationRecruitingNCT07094035Not applicable1 country
- Comparison of Rimegepant and Placebo for Pain in IBSCompletedNCT06221111Phase 21 country
- (FODMAP) Diet on Improving Symptoms of Patients With Irritable Bowel SyndromeCompletedNCT07299305Not applicable1 country
- Basket Study (CT-100-002) to Evaluate the Effects of a DiNaMo™ Component TrainingCompletedNCT05573685Not applicable1 country
- Dieta Mediterranea e Sindrome Dell'Intestino Irritabile in Pazienti PediatriciStatus unknownNCT05738343
- Clinical Effectiveness of Exposure Based Cognitive Behavioral Group Therapy for IBSCompletedNCT04756414Not applicable
- Effect of Curcumin on Gut Microbiota in IBSCompletedNCT03568513Not applicable1 country
- Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrome in the Russian FederationCompletedNCT035491431 country
- International Psychometric Validation Study of the Intestinal Gas Questionnaire (IGQ)CompletedNCT030025843 countries
- Neuroimaging and Biomarkers in Chronic Visceral PainCompletedNCT01602575Not applicable1 country
- Proposal Evaluating Time-specific Relationships Between Variables of Pain, Stress, and Bloating in IBS Diarrhea and Constipation Symptoms Using a Palm PilotCompletedNCT00619125
- The Prevalence of Irritable Bowel Syndrome Using Rome IV Criteria in Medical Student and The Related FactorsCompletedNCT031788771 country
- Effects of Wheat Breads on Symptoms of IBS, a Pilot StudyCompletedNCT02572908Not applicable1 country
- Effect of Two Different Rye Bread Types in Irritable Bowel SyndromeCompletedNCT02161120Not applicable1 country
- Effects of ROSE-010 on GI Transit in Constipation Predominant Irritable Bowel Syndrome (C-IBS) PatientsCompletedNCT01056107Phase 1/21 country
- Cheno Effect on Transit in Health and IBS-CCompletedNCT00912301Phase 21 country
- Mindfulness vs. Support Groups for Irritable Bowel SyndromeCompletedNCT00680693Not applicable1 country
- Efficacy Study of Rezular (Arverapamil) in the Treatment of Irritable Bowel Syndrome With Diarrhea (IBS-D)CompletedNCT00552565Phase 31 country
- 8 Weeks Treatment With DDP225 in Patients With Diarrhea Predominant IBSCompletedNCT00230581Phase 22 countries