Pilot Study of Curcumin Formulation and Ashwagandha Extract in Advanced Osteosarcoma (OSCAT)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2011 by Tata Memorial Hospital.
Recruitment status was  Recruiting
Pharmanza Herbals Pvt Limited (PHPL)
Information provided by:
Tata Memorial Hospital
ClinicalTrials.gov Identifier:
First received: May 23, 2008
Last updated: June 22, 2011
Last verified: June 2011
Curcumin as well as the ashwagandha extract are ingredients from traditional indian medicine and have been shown to be potent anti-cancer compounds in laboratory as well as animal studies. This study will test the safety and efficacy of a curcumin formulation and the ashwagandha extract in high grade relapsed or metastatic osteosarcoma where no other second line chemotherapy is being given. The pharmacokinetics will be studied along with response as measured on CT scans and PET scans as well as the quality of life and any toxicity.

Condition Intervention Phase
Dietary Supplement: Curcumin powder
Dietary Supplement: Ashwagandha extract
Phase 1
Phase 2

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Evaluation of Curcumin Formulation, and Ashwagandha Root Powder Extract in the Management of Advanced High Grade Osteosarcoma"

Resource links provided by NLM:

Further study details as provided by Tata Memorial Hospital:

Primary Outcome Measures:
  • response, toxicity, disease progression [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • quality of life [ Time Frame: 2 years ] [ Designated as safety issue: No ]

Estimated Enrollment: 24
Study Start Date: May 2008
Estimated Study Completion Date: June 2013
Estimated Primary Completion Date: June 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: C
Dietary Supplement: Curcumin powder
oral capsules containing the investigational agent
Other Name: M3CX,
Experimental: A
Ashwagandha extract
Dietary Supplement: Ashwagandha extract
4.5% extract of ashwagandha
Other Names:
  • Withania somnifera,
  • Dunal,
  • Indian Ginseng

Detailed Description:

Eligibility criteria

  1. Osteosarcoma which has relapsed after treatment and for which no second line chemotherapy is planned and in which disease is not amenable to surgery.
  2. Patient should be able to follow-up 3 monthly for clinical and imaging assessment as well as biochemical tests

Ages Eligible for Study:   8 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patients (between the ages of 8 to 65 years) with histologically proven high grade osteosarcoma of the extremity and relapsed disease after primary line of treatment who are unsuitable or refuse secondary chemotherapy.
  • Patients with advanced disease unable or unwilling to take primary conventional treatment
  • Patients with early or non-metastatic disease who are unable or unwilling to take the standard chemotherapy.
  • Adequate hepatic function defined by total bilirubin not more than 1.5 times the upper limit of normal (ULN) and SGOT and SGPT not more than 2.5 times the (ULN)
  • Adequate renal function defined by the creatinine clearance greater than 50 ml/min, calculated by cockcroft-Gault formula

Exclusion Criteria:

  • Patients who are suitable for second line chemotherapy and can afford it
  • Age less than 8 years or greater than 65 years
  • Pregnant or lactating women
  • Patients who are unable or unwilling to provide blood samples for the drug assays.
  • Low grade osteosarcoma
  • Patient requiring treatment with CYP3A4 inducers or inhibitors (patients on treatment for epilepsy or tuberculosis)
  • Participation in any investigational drug study within 28 days prior to study treatment.
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00689195

Contact: Manish Agarwal, M.S(Orth), D.N.B(Orth) 91-22-2444-7189 mgagarwal@gmail.com
Contact: Vikram S Gota, M.D 91-22-2417-7000 ext 4537 vikramgota@gmail.com

Tata Memorial Hospital Recruiting
Mumbai, Maharashtra, India, 400012
Contact: Manish Agarwal, M.S(Orth)    91-22-2444-7189    mgagarwal@gmail.com   
Contact: Vikram S Gota, M.D    91-22-2417-7000 ext 4537    vikramgota@gmail.com   
Principal Investigator: Manish Agarwal, M.S(Orth)         
Sponsors and Collaborators
Tata Memorial Hospital
Pharmanza Herbals Pvt Limited (PHPL)
  More Information

Responsible Party: Dr Manish Agarwal, Tata Memorial Hospital
ClinicalTrials.gov Identifier: NCT00689195     History of Changes
Other Study ID Numbers: 381 
Study First Received: May 23, 2008
Last Updated: June 22, 2011
Health Authority: India: Drugs Controller General of India

Keywords provided by Tata Memorial Hospital:
Pharmacokinetics of curcumin and ashwagandha formulation

Additional relevant MeSH terms:
Neoplasms by Histologic Type
Neoplasms, Bone Tissue
Neoplasms, Connective Tissue
Neoplasms, Connective and Soft Tissue
Analgesics, Non-Narcotic
Anti-Inflammatory Agents
Anti-Inflammatory Agents, Non-Steroidal
Antineoplastic Agents
Antirheumatic Agents
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Peripheral Nervous System Agents
Physiological Effects of Drugs
Sensory System Agents

ClinicalTrials.gov processed this record on May 24, 2016