CTRI/2018/04/013086
Active, not recruiting
未知
A prospective, open label, pilot, study to evaluate efficacy, safety and bio- availability of oral Arsenic compound prepared by Ayurvedic method (Somal- NTAX-44) in patients with solid tumours.
ConditionsHealth Condition 1: C00-D49- Neoplasms
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: C00-D49- Neoplasms
- Sponsor
- Rasayani Biologics Pvt Ltd
- Status
- Active, not recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Male or female patient with solid tumours aged 20 to 70 of solid tumours
- •All those patients who have not responded to conventional anticancer therapies.
- •Cancer Patients who are not willing to take chemotherapy
- •Cancer patients who are eligible to receive treatment of Somal.
- •Cancer Patients who has expected survival of more than 3 months
Exclusion Criteria
- •1\.Patients taking Chemotherapy.
- •2\.Patients taking conventional products containing Arsenic.
- •3\.Patient with deranged hepatic or renal profile at baseline.
- •4\.Patients with Pre\-existing cardiac illness.
- •5\.Patients who has ECOG performance is \>\= 2\.
Outcomes
Primary Outcomes
Not specified
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