Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
CellCentric Ltd.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Provision of consent
ECOG performance status 0-1
Assessable disease (by CT, MRI, bone scan or X-ray)
Adequate organ function
Highly effective contraception measures for duration of study
Previously received abiraterone and/or enzalutamide (or equivalent anti-androgen), and docetaxel (unless ineligible or refused)
Progressive disease documented by one or more of the following:
* Biochemical progression defined as at least 2 stepwise increases in a series of any 3 PSA values
* Progression as defined by RECIST v1.1 guideline for assessment of malignant soft tissue disease.
* Progression defined as two or more new metastatic bone lesions confirmed on bone scan from a previous assessment
PSA at screening ≥2 μg/L
Serum testosterone concentration ≤50 ng/dL
Serum albumin \>2.5 g/dL
Patients must have previously progressed on abiraterone treatment
Patients whose last dose of abiraterone is greater than 6 months prior to start of study treatment will receive a 4-week run-in treatment with abiraterone to confirm refractoriness to abiraterone treatment
Patients must have previously progressed on enzalutamide treatment
Patients whose last dose of enzalutamide is greater than 6 months prior to start of study treatment will receive a 4-week run-in treatment with enzalutamide to confirm refractoriness to enzalutamide treatment
Advanced solid tumour with identification of markers which may indicate potential for response to p300/CBP inhibition. Markers include loss of function mutations in CREBBP, EP300 or ARID1A, MYC gene amplifications or rearrangements and androgen receptor (AR) gene amplifications or over-expression.
You may not be if
Intervention with any chemotherapy, investigational agents or other anti-cancer drugs within 14 days or 5 half-lives of the first dose
Radiotherapy with a wide field of radiation or to more than 30% of the bone marrow within 4 weeks of the first dose of study treatment
Major surgical procedure or significant traumatic injury within 4 weeks of the first dose of study treatment
Strong inhibitors of CYP3A4 or CYP3A4 substrates with a narrow therapeutic range taken within 2 weeks of the first dose of study treatment
Strong inducers of CYP3A4 within 4 weeks of the first dose of study treatment
Statins; patients should discontinue statins prior to starting study treatment
Any unresolved reversible toxicities from prior therapy \>CTCAE grade 1 at the time of starting study treatment
Any evidence of severe or uncontrolled systemic diseases
Any known uncontrolled inter-current illness
QTcF prolongation (\> 480 msec).
Primary brain tumours or known or suspected brain metastases.
Clinically significant cardiac abnormalities
History of seizures or other predisposing factors
Use of substrates with a narrow therapeutic index metabolised by CYP2C9 or CYP2C19 within 2 weeks of the first dose of study treatment
Clinically significant cardiac abnormalities
Clareo Health | Study to Evaluate CCS1477 in Advanced Tumours
