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NCT Number: NCT00086216

Safety and Efficacy of Atiprimod for Patients With Refractory Multiple Myeloma

This is a Phase I/IIa clinical trial to identify the maximum tolerated dose of atiprimod and to evaluate the safety of atiprimod in patients with refractory or relapsed multiple myeloma.

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Key information

About this study

This is a multi-center, open-label, dose escalation study intended to identify the MTD of atiprimod alone and the MTD of atiprimod when given in combination with ursodiol. The atiprimod dose will be escalated in sequential cohorts. Ten dose levels of atiprimod are planned for the atiprimod alone dose escalation: 30, 60, 90, 120, 180, 240, 300, 360, 420, and 480 mg/day to be given orally. Six dose levels of atiprimod are planned for the atiprimod in combination with ursodiol dose escalation: 180, 240, 300, 360, 420, and 480 mg/day to be given orally. The dose of ursodiol will remain constant for all cohorts (300 mg ursodiol orally three times a day everyday). Up to 105 patients will participate depending on the level at which toxicity is observed. Patients will be assigned to dose level in the order of study entry.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • documented history of multiple myeloma,
  • failed at least two prior regimens for multiple myeloma,
  • 18 years of age or older,
  • ECOG(Zubrod)PS of 0 to 2,
  • screening evaluation for determining eligibility prior to enrollment,
  • signed informed consent form,

Exclusion criteria

  • concomitant therapy medications including corticosteroids or other chemotherapy that is or may be active against myeloma ,
  • renal insufficiency (serum creatinine levels of > 2mg/dL),
  • mucosal bleeding,
  • any condition which in the opinion of the Investigator, places the patient at unacceptable risk if he/she were to participate in the study.
  • clinically relevant active infection or co-morbid medical conditions.
  • prior malignancy(within the last 3 years) except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer for which the patient is has been disease-free for at least 3 years.
  • patients with non-secretory myeloma.
  • as atiprimod is a potent inhibitor or CYP2D6, patients taking drugs that are substrates of CYP2D6(e.g. beta blockers, antidepressants and antipsychotics) will be excluded.

Treatment and study plan

Atiprimod

Drug

Oral, once a day, 14 days on 14 days off

Primary outcomes

  1. The primary objective of this study is to identify the maximum tolerated dose

    Time frame: 1 year

Secondary outcomes

  1. The secondary objective of this study is to measure the pharmacokinetics of

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

Callisto Pharmaceuticals

Industry

Registry information

Official study title

An Open-Label Study of the Safety and Efficacy of Atiprimod Treatment for Patients With Refractory or Relapsed Multiple Myeloma

Important dates

Study start
2004
Study completion
2007
First posted
Jun 30, 2004
Registry last updated
Dec 21, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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