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NCT00947739 · ClinicalTrials.gov registry record · Phase 1

Phase I and Pharmacology Study of Camptothecin-20-O-Propionate Hydrate (CZ48) in Patients With Solid Tumors or Lymphoma

A Phase 1 study, sponsored by New Mexico Cancer Research Alliance.

Completed
Registry status
Phase 1
Development phase
43
Enrollment target

NCT00947739: Completed Phase 1 study, sponsored by New Mexico Cancer Research Alliance.

NCT00947739 is a Phase 1 study that has completed, run by New Mexico Cancer Research Alliance. The registered enrollment target is 43 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00947739, a Phase 1 study, has completed, sponsored by New Mexico Cancer Research Alliance.

COMPLETED
Registry status
Phase 1
Development phase
43 participants
Enrollment target

Study Summary

This is a phase I and pharmacology study of Camptothecin-20-O-Propionate Hydrate (CZ48) in Patients with Solid Tumors or Lymphoma. OBJECTIVES Primary: 1. To describe the dose limiting toxicities and adverse event profile of Camptothecin-20-O-Propionate hydrate (CZ48) administered orally every day. 2. To determine Phase II recommended dose of Camptothecin-20-O-Propionate hydrate (CZ48) administered orally every day. Secondary: 3. To perform a pharmacokinetic study of orally administered CZ48 in the plasma. 4. To assess responses by RECIST criteria. 5. To follow patients for survival.

Interventions

  • DRUG Camptothecin-20-O-Propionate Hydrate (CZ48)

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2008-09
Est. Completion 2014-03
Phase Phase 1

What the finished NCT00947739 record still lists

NCT00947739 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower).

The record links to 0 conditions, and to 1 intervention - of which Camptothecin-20-O-Propionate Hydrate (CZ48) is the first listed.

NCT00947739 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00947739 about?

NCT00947739 is a clinical study titled "Phase I and Pharmacology Study of Camptothecin-20-O-Propionate Hydrate (CZ48) in Patients With Solid Tumors or Lymphoma". This is a phase I and pharmacology study of Camptothecin-20-O-Propionate Hydrate (CZ48) in Patients with Solid Tumors or Lymphoma. OBJECTIVES Primary: 1. To describe the dose limiting toxicities and adverse event profile of Camptothecin-20-O-Propionate hydrate (CZ48) administered orally every day...

What is the current status of trial NCT00947739?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 43 participants. The study started on 2008-09. Estimated completion is 2014-03.

What interventions are being tested in trial NCT00947739?

The interventions under investigation include: Camptothecin-20-O-Propionate Hydrate (CZ48) (DRUG).

Who is sponsoring clinical trial NCT00947739?

This trial is sponsored by New Mexico Cancer Research Alliance, which has 66 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00947739's enrollment target sits among peer trials

43 1100th of 2000 higher than 896 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

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Source: ClinicalTrials.gov NCT00947739, the US trial registry maintained by the National Library of Medicine. NCT00947739 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.