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NCT00258258 · ClinicalTrials.gov registry record · Phase 1

Paricalcitol and Zoledronate in Treating Patients With Relapsed or Refractory Multiple Myeloma or Other Plasma Cell Disorders

A Phase 1 study, sponsored by Roswell Park Cancer Institute.

Terminated
Registry status
Phase 1
Development phase
7
Enrollment target

NCT00258258: Clinical Trial Phase 1 study, sponsored by Roswell Park Cancer Institute.

NCT00258258 is a Phase 1 study that was terminated before completion, run by Roswell Park Cancer Institute. The registered enrollment target is 7 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00258258, a Phase 1 study, was terminated before completion, sponsored by Roswell Park Cancer Institute.

TERMINATED
Registry status
Phase 1
Development phase
7 participants
Enrollment target

Study Summary

RATIONALE: Paricalcitol may cause multiple myeloma cells to look more like normal cells, and to grow and spread more slowly. Paricalcitol may also stop the growth of the cancer cells by blocking blood flow to the cancer. Zoledronate may delay or prevent bone metastases in patients with multiple myeloma. Giving paricalcitol together with zoledronate may be an effective treatment for multiple myeloma or other plasma cell disorders. PURPOSE: This clinical trial is studying the side effects and best dose of paricalcitol when given with zoledronate in treating patients with relapsed or refractory multiple myeloma or other plasma cell disorders.

Interventions

  • DRUG zoledronic acid
  • DRUG paricalcitol

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2005-08
Phase Phase 1
Roswell Park Cancer Institute

365 total trials

Why NCT00258258 stopped before completion

NCT00258258 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (88% lower).

The record links to 0 conditions, and to 2 interventions - of which zoledronic acid is the first listed.

NCT00258258 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00258258 about?

NCT00258258 is a clinical study titled "Paricalcitol and Zoledronate in Treating Patients With Relapsed or Refractory Multiple Myeloma or Other Plasma Cell Disorders". RATIONALE: Paricalcitol may cause multiple myeloma cells to look more like normal cells, and to grow and spread more slowly. Paricalcitol may also stop the growth of the cancer cells by blocking blood flow to the cancer. Zoledronate may delay or prevent bone metastases in patients with multiple myel...

What is the current status of trial NCT00258258?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 7 participants. The study started on 2005-08.

What interventions are being tested in trial NCT00258258?

The interventions under investigation include: zoledronic acid (DRUG), paricalcitol (DRUG).

Who is sponsoring clinical trial NCT00258258?

This trial is sponsored by Roswell Park Cancer Institute, which has 365 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00258258's enrollment target sits among peer trials

7 1972nd of 2000 higher than 27 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 NCT00258258, the US trial registry maintained by the National Library of Medicine. NCT00258258 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.