Human study PLS-00001
Phase II trial of PL 14736 (BPC-157) enema in mild-to-moderate ulcerative colitis
Version 1 · published November 7, 2026 · evidence through November 7, 2026 · research snapshot 2026.1.1 · methodology ev-1 · Automated assessment by AI (claude-opus-5-5 and claude-sonnet-5-5), not reviewed by a person.
Only the abstract was available. Essential methods may be missing, which limits what can be judged.
Reports of this study
Every publication, registration and abstract describing this one study. Participants are counted once.
- Ruenzi M, et al. A Multicenter, Randomized, Double Blind, Placebo-Controlled Phase II Study of PL 14736 Enema in the Treatment of Mild-to-Moderate Ulcerative Colitis. Gastroenterology. 2005;128:A584 (meeting abstract).conference abstract
Design and participants
- Design
- Randomized controlled trial
- Population
- Patients with mild-to-moderate ulcerative colitis
- Conditions
- Ulcerative colitis
- Setting
- Multicenter
- Planned enrollment (registry)
- Not reported
- Enrolled
- Not reported
- Randomized
- Not reported
- Completed follow-up
- Not reported
Intervention and comparator
What each group received. Related peptides, analogs and combinations are never treated as the compound itself.
- PL 14736 enema (intervention) · bpc-157 · PL 14736 (BPC-157) given as an enema · rectal (enema) · Not reported assigned
- Placebo enema (comparator) · Placebo · placebo · rectal (enema) · Not reported assigned
What the authors reported
As stated in the sources. This is the authors’ account, not Peptide Library’s assessment.
Adverse events
None reported. That is not evidence of safety, and how safety was monitored isn’t described.
Peptide Library’s assessment
An automated assessment, made by AI separately from the authors’ conclusions and not reviewed by a person. How risk of bias is assessed.
Limitations
- abstract only: Only a bibliographic citation of a meeting abstract is available. There is no abstract text, so methods, sample size, outcomes and results cannot be assessed.
- selective reporting: No results, outcomes or adverse events are reported in the record. Nor is there any indication of full publication or registration, so reporting completeness cannot be verified.
- small or imprecise: Sample size and arm sizes are not stated in the record, so the precision of any findings cannot be judged.
No risk-of-bias assessment has been published for this study’s results.
Claims this study informs
- Reduces knee pain: not eligible (wrong population) for “Knee pain intensity”
- Supports tendon injury recovery: not eligible (wrong population) for “Function and return to activity”
- Improves muscle injury recovery: not eligible (wrong population) for “Time to return to activity”
- Improves gastrointestinal conditions: not eligible (insufficient data) for “Clinical response or remission”
- Is safe for human administration: not eligible (insufficient data) for “Adverse events, serious adverse events and discontinuations”
Where each value comes from
- arms: EXTERNAL report-1, citation (study title within citation) · extracted by AI (automated, not verified by a person) · abstract only
- design: EXTERNAL report-1, citation (study title within citation) · extracted by AI (automated, not verified by a person) · abstract only
- limitations: EXTERNAL report-1, citation (meeting abstract designation in citation) · extracted by AI (automated, not verified by a person) · abstract only
- population: EXTERNAL report-1, citation (study title within citation) · extracted by AI (automated, not verified by a person) · abstract only
Version 1 · published November 7, 2026 · evidence through November 7, 2026 · research snapshot 2026.1.1 · methodology ev-1 · Automated assessment by AI (claude-opus-5-5 and claude-sonnet-5-5), not reviewed by a person.
These assessments describe published research. Records marked automated were produced by AI under the published methodology and have not been reviewed by a person; they can contain errors. None of this is medical advice, not a statement about any product’s safety for human use, and not a regulatory approval. Peptide Library’s vendor and partner relationships play no part in them (editorial independence).