Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:57 PM
Ignite Modification Date:
2025-12-24 @ 4:57 PM
NCT ID:
NCT02263950
Eligibility Criteria:
Inclusion Criteria:
1. Subjects of 18 years or older at the Screening Visit.
2. Histologic and/or cytologically confirmed diagnosis of solid tumour with clinical and imaging evidence that the tumour is advanced and for whom there is no effective standard therapy available.
3. At least one evaluable tumour that is at least 10 mm by computerised tomography (CT) scan or magnetic resonance imaging (MRI) at the pre-treatment stage
4. At least one prior systemic anti-cancer treatment and disease that is refractory or progressive following treatment.
5. Eastern Co operative Oncology Group (ECOG) performance ≤ 2.
6. An adequate renal, liver and bone marrow function.
7. Women of child bearing potential (WOCBP) must have a negative pregnancy test before the start of treatment.
8. Sexually active women of childbearing potential must be using an acceptable form of contraception, as detailed in the protocol.
9. Male subjects must have had a successful vasectomy (confirmed azoospermia) or they and their female partner must meet the criteria defined in the protocol (i.e., not of childbearing potential or practicing highly effective contraception throughout the study period and for 30 days after study drug discontinuation). Those with partners using hormonal contraceptives must also be using an additional approved method of barrier contraception.
10. Expected life expectancy \> 4 months.
Exclusion Criteria:
1. Unwillingness or inability to provide informed consent.
2. Any evidence of severe or uncontrolled systemic diseases, infection or laboratory finding that in the view of the Investigator makes it undesirable for the patient to participate in the trial.
3. Allergic to artemether or other artemisinin derivatives or any of the components of the sublingual formulation.
4. Pregnancy or lactation.
5. Subject had major surgery or significant traumatic injury within 4 weeks of start of study drug; subject has not recovered from the side effects of any major surgery (defined as requiring general anaesthesia) or subject might require major surgery during the course of the study.
6. Subject has had anti-cancer treatment within 4 weeks of start of study drug, excluding small field palliative irradiation which may be performed up to 2 weeks prior to start of study drug.
7. Subject has had prior treatment with any investigational drug within the preceding 4 weeks before study start.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02263950
Study Brief:
Protocol Section:
NCT02263950