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

NCT00113841 · ClinicalTrials.gov registry record · NA

Curcumin (Diferuloylmethane Derivative) With or Without Bioperine in Patients With Multiple Myeloma

A NA study of Multiple Myeloma, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
NA
Development phase
42
Enrollment target
1
Study location

NCT00113841: Completed NA study of Multiple Myeloma, sponsored by M.D. Anderson Cancer Center.

NCT00113841 is a NA study of Multiple Myeloma that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 42 participants, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT00113841, a NA study of Multiple Myeloma, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
NA
Development phase
42 participants
Enrollment target
1
Study location

Study Summary

Primary Objectives: 1. To evaluate clinical tolerance and response to curcumin alone and in combination with Bioperine in patients with multiple myeloma. 2. To compare the pharmacokinetics and pharmacodynamics of curcumin and curcumin + Bioperine and evaluate the effect of Bioperine on the bioavailability of curcumin. 3. To evaluate the biologic effects of curcumin alone and in combination with Bioperine on the expression of NF-kB and related genes in the Multiple Myeloma (MM) cells.

Primary Outcome

Percent change of NF-kB =\[(expression at 4 weeks- expression at baseline)/expression at baseline\]\*100%. Bone marrow aspirate/biopsy for expression of NF-kB and related genes/proteins markers at baseline and after 4 weeks.

Conditions Studied

Interventions

  • DRUG Curcumin
  • DRUG Bioperine

Study Locations (1)

Texas

  • U.T.M.D. Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2004-11
Est. Completion 2009-08
Phase NA
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT00113841 record still lists

NCT00113841 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (92% lower).

The record links to 1 condition, with Multiple Myeloma appearing as the primary indexed condition, and to 2 interventions - of which Curcumin is the first listed.

NCT00113841 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT00113841 about?

NCT00113841 is a clinical study titled "Curcumin (Diferuloylmethane Derivative) With or Without Bioperine in Patients With Multiple Myeloma". Primary Objectives: 1. To evaluate clinical tolerance and response to curcumin alone and in combination with Bioperine in patients with multiple myeloma. 2. To compare the pharmacokinetics and pharmacodynamics of curcumin and curcumin + Bioperine and evaluate the effect of Bioperine on the bioavail...

What is the current status of trial NCT00113841?

This trial is currently completed. It is a NA study. The enrollment target is 42 participants. The study started on 2004-11. Estimated completion is 2009-08.

What conditions does trial NCT00113841 study?

This clinical trial studies the following conditions: Multiple Myeloma.

What interventions are being tested in trial NCT00113841?

The interventions under investigation include: Curcumin (DRUG), Bioperine (DRUG).

Who is sponsoring clinical trial NCT00113841?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00113841 being conducted?

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

Similar trials for Multiple Myeloma

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 NCT00113841's enrollment target sits among peer trials

42 282nd of 438 higher than 155 of 438 other Multiple Myeloma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Multiple Myeloma 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

  • NCT02852213 · 42 participants · Phase 1

    A Single-Stage, Adaptive, Open-label, Dose Escalation Safety and Efficacy Study of AADC Deficiency in Pediatric Patients

  • NCT03136146 · 42 participants · Phase 2

    Combination Chemotherapy in Treating Patients With Relapsed or Refractory Acute Lymphoblastic Leukemia, Lymphoblastic Lymphoma, Burkitt Lymphoma/Leukemia, or Double-Hit Lymphoma/Leukemia

  • NCT03178149 · 42 participants · Phase 1

    A Study of the Safety and Tolerability of ASP7317 in Senior Adults Who Are Losing Their Clear, Sharp Central Vision Due to Geographic Atrophy Secondary to Dry Age-related Macular Degeneration

  • NCT03663530 · 42 participants · NA

    Circadian Misalignment and Energy Balance

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00113841, the US trial registry maintained by the National Library of Medicine. NCT00113841 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.