Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00571727 · ClinicalTrials.gov registry record · Phase 2

Long-Term Treatment With rhIGF-1 in GHIS

A Phase 2 study, sponsored by Ipsen.

Completed
Registry status
Phase 2
Development phase
92
Enrollment target

NCT00571727: Completed Phase 2 study, sponsored by Ipsen.

NCT00571727 is a Phase 2 study that has completed, run by Ipsen. The registered enrollment target is 92 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (31% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00571727, a Phase 2 study, has completed, sponsored by Ipsen.

COMPLETED
Registry status
Phase 2
Development phase
92 participants
Enrollment target

Study Summary

The objective of this study was to evaluate the long-term safety and effectiveness of mecasermin (the study drug) in children with growth failure due to severe Primary insulin-like growth factor-1 deficiency (Primary IGFD).

Primary Outcome

Height velocity is the difference between 2 height measurements, divided by years elapsed between measurements.

Interventions

  • DRUG mecasermin

Trial Details

FieldValue
Enrollment Target 92 participants
Start Date 1991-05-20
Est. Completion 2011-12-15
Phase Phase 2
Ipsen

85 total trials

What the finished NCT00571727 record still lists

NCT00571727 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 92 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (31% lower).

The record links to 0 conditions, and to 1 intervention - of which mecasermin is the first listed.

NCT00571727 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00571727 about?

NCT00571727 is a clinical study titled "Long-Term Treatment With rhIGF-1 in GHIS". The objective of this study was to evaluate the long-term safety and effectiveness of mecasermin (the study drug) in children with growth failure due to severe Primary insulin-like growth factor-1 deficiency (Primary IGFD).

What is the current status of trial NCT00571727?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 92 participants. The study started on 1991-05-20. Estimated completion is 2011-12-15.

What interventions are being tested in trial NCT00571727?

The interventions under investigation include: mecasermin (DRUG).

Who is sponsoring clinical trial NCT00571727?

This trial is sponsored by Ipsen, which has 85 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00571727's enrollment target sits among peer trials

92 767th of 2000 higher than 1,230 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03184545 · 92 participants · Phase 3

    Comparing the Outcome of Electrical Stimulation and Physical Therapy in Patellofemoral Pain Syndrome

  • NCT04172532 · 92 participants · Phase 1

    Testing the Addition of a New Anti-cancer Drug, M3814 (Peposertib), to the Usual Radiotherapy in Patients With Locally Advanced Pancreatic Cancer

  • NCT04508088 · 92 participants

    Skeletal Health and Bone Marrow Composition in Newly Diagnosed Adolescents With Crohn Disease

  • NCT04840602 · 92 participants · Phase 2

    Testing the Combination of Venetoclax and Rituximab, in Comparison to the Usual Treatment (Ibrutinib Plus Rituximab or Zanubrutinib Alone) for Waldenstrom's Macroglobulinemia/Lymphoplasmacytic Lymphoma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT00571727, the US trial registry maintained by the National Library of Medicine. NCT00571727 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.