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NCT05670951

A Multi-center, Double-Blind, Randomized, Two-Arm, Parallel-Group, Placebo Controlled Study to Assess the Efficacy and Safety of ELGN-2112 on Intestinal Malabsorption in Preterm Infants

Recruiting now Phase 3 Last updated 22 January 2026
What this trial tests

Phase 3 trial testing ELGN-2112 in Intestinal Malabsorption in 360 participants. Currently enrolling.

Timeline
27 February 2025
Primary endpoint
1 November 2027
1 May 2029

Quick facts

Lead sponsorElgan Pharma Ltd.
PhasePhase 3
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment360
Start date27 February 2025
Primary completion1 November 2027
Estimated completion1 May 2029
Sites1 location across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Elgan Pharma Ltd. — full company profile →

Who can join

Adults 1 Day to 5 Days, any sex, with Intestinal Malabsorption. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The study will evaluate the effect of ELGN-2112 on intestinal malabsorption in preterm infants.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Elgan Pharma Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05670951.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing