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NCT03301038 · ClinicalTrials.gov registry record · Phase 2

Rifampin in CYP24A1-related Hypercalcemia and Hypercalciuria

A Phase 2 study of Genetic Disease and Hypercalciuria, sponsored by Children's Hospital of Philadelphia.

Recruiting
Registry status
Phase 2
Development phase
60
Enrollment target
1
Study location

NCT03301038: Recruiting Phase 2 study of Genetic Disease and Hypercalciuria, sponsored by Children's Hospital of Philadelphia.

NCT03301038 is a Phase 2 study of Genetic Disease and Hypercalciuria that is actively recruiting participants, run by Children's Hospital of Philadelphia. The registered enrollment target is 60 participants, below the 2,559-participant average among 30 other Genetic Disease trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03301038, a Phase 2 study of Genetic Disease and Hypercalciuria, is actively recruiting participants, sponsored by Children's Hospital of Philadelphia.

RECRUITING
Registry status
Phase 2
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

This study evaluates the efficacy of rifampin in the treatment of hypercalcemia and/or hypercalciuria in participants with at least one inactivating mutation of the CYP24A1 gene. Eligible subjects will receive rifampin for a total of 16 weeks during this study.

Primary Outcome

Measured at baseline and every 4 weeks

Interventions

  • DRUG Rifampin

Study Locations (1)

Pennsylvania

  • Children's Hospital of Philadelphia - Philadelphia

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2018-07-25
Est. Completion 2030-12
Phase Phase 2
Children's Hospital of Philadelphia

431 total trials

What NCT03301038 shows while recruiting

NCT03301038 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 2,559-participant average among 30 other Genetic Disease trials with a reported enrollment target (98% lower).

The record links to 6 conditions, with Genetic Disease appearing as the primary indexed condition, and to 1 intervention - of which Rifampin is the first listed.

NCT03301038 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT03301038 about?

NCT03301038 is a clinical study titled "Rifampin in CYP24A1-related Hypercalcemia and Hypercalciuria". This study evaluates the efficacy of rifampin in the treatment of hypercalcemia and/or hypercalciuria in participants with at least one inactivating mutation of the CYP24A1 gene. Eligible subjects will receive rifampin for a total of 16 weeks during this study.

What is the current status of trial NCT03301038?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2018-07-25. Estimated completion is 2030-12.

What conditions does trial NCT03301038 study?

This clinical trial studies the following conditions: Genetic Disease, Hypercalciuria, Idiopathic Infantile Hypercalcaemia - Severe Form, Hypercalcemia, Idiopathic, of Infancy, Hypercalciuric Hypercalcemia.

What interventions are being tested in trial NCT03301038?

The interventions under investigation include: Rifampin (DRUG).

Who is sponsoring clinical trial NCT03301038?

This trial is sponsored by Children's Hospital of Philadelphia, which has 431 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03301038 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Genetic Disease

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03301038's enrollment target sits among peer trials

60 24th of 30 higher than 7 of 30 other Genetic Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Genetic Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03301038, the US trial registry maintained by the National Library of Medicine. NCT03301038 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.