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

NCT01380756 · ClinicalTrials.gov registry record · Phase 1

Study Evaluating Orally Administered AMG 900 in Adult Subjects With Acute Myeloid Leukemia

A Phase 1 study, sponsored by Amgen.

Completed
Registry status
Phase 1
Development phase
35
Enrollment target

NCT01380756: Completed Phase 1 study, sponsored by Amgen.

NCT01380756 is a Phase 1 study that has completed, run by Amgen. The registered enrollment target is 35 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01380756, a Phase 1 study, has completed, sponsored by Amgen.

COMPLETED
Registry status
Phase 1
Development phase
35 participants
Enrollment target

Study Summary

This study of AMG 900 will be conducted in two parts: dose escalation and dose expansion. The dose escalation part of the study is aimed at evaluating the safety, tolerability and PK (pharmacokinetics) of oral AMG 900 in subjects with acute myeloid leukemia. Up to 93 subjects may be enrolled in dose escalation. The dose expansion part of the study will consist of 20 subjects with acute myeloid leukemia. The dose of AMG 900 will be dependent upon data from the dose escalation part of the study.

Interventions

  • DRUG Arm 1- Dose Escalation
  • DRUG Arm 2- Dose Expansion

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2011-10-04
Est. Completion 2014-09-04
Phase Phase 1
Amgen

558 total trials

What the finished NCT01380756 record still lists

NCT01380756 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower).

The record links to 0 conditions, and to 2 interventions - of which Arm 1- Dose Escalation is the first listed.

NCT01380756 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01380756 about?

NCT01380756 is a clinical study titled "Study Evaluating Orally Administered AMG 900 in Adult Subjects With Acute Myeloid Leukemia". This study of AMG 900 will be conducted in two parts: dose escalation and dose expansion. The dose escalation part of the study is aimed at evaluating the safety, tolerability and PK (pharmacokinetics) of oral AMG 900 in subjects with acute myeloid leukemia. Up to 93 subjects may be enrolled in dose...

What is the current status of trial NCT01380756?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 35 participants. The study started on 2011-10-04. Estimated completion is 2014-09-04.

What interventions are being tested in trial NCT01380756?

The interventions under investigation include: Arm 1- Dose Escalation (DRUG), Arm 2- Dose Expansion (DRUG).

Who is sponsoring clinical trial NCT01380756?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01380756's enrollment target sits among peer trials

35 1258th of 2000 higher than 728 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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

  • NCT01697371 · 35 participants · NA

    Proton Therapy in the Treatment of Liver Metastases

  • NCT01940757 · 35 participants · Phase 1

    Experimental Infection of Hookworm-naïve Adults With Dermally-applied Infectious Necator Americanus Hookworm Larvae

  • NCT02235857 · 35 participants · NA

    Post Approval Study of Liposorber LA-15 System for the Treatment of Focal Segmental Glomerulosclerosis in Children

  • NCT02637934 · 35 participants · Phase 1

    Phase I Pilot Study of Biodistribution, Metabolism and Excretion of Novel Radiotracer [18F]Fluorthanatrace (FTT) by PET/CT

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 NCT01380756, the US trial registry maintained by the National Library of Medicine. NCT01380756 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.