Safety Study of SLC-0111 in Subjects With Advanced Solid Tumours

NCT02215850 | Completed Phase 1

• 1 other identifier: OZM-055/SLC0111-14-C01
• Study Type: interventional
• Target: 24
• Locations: 1 country
• Sites: 3

Brief Summary

SLC-0111 is a selective, small molecule, inhibitor of carbonic anhydrase (CA) IX and is in development for the treatment of solid tumours over-expressing CA IX. CAIX, a transmembrane metalloenzyme, is overexpressed on extracellular surfaces of hypoxic tumour cells but its expression is highly restricted in normal tissue. CAIX is a functional regulator of processes critical for tumour growth and metastasis, including pH regulation, survival, migration and invasion. This prospective single arm study will evaluate the safety of SLC-0111 given once daily in 28 day cycles in subjects with advanced solid tumours. The intent of this research study is to find our more information such as: the highest dose of SLC-0111 that can be given safely, the side effect it may cause, to examine how the body affects the study drug concentration in the blood (pharmacokinetics or PK), and to gain some information on its effectiveness in treating cancer.

Conditions

Solid Tumours

Outcome Measures

Primary Outcomes (1)

• Number of participants with adverse events

  To evaluate the safety and tolerability of SLC-0111, administered once daily, in subjects with advanced solid tumours.

  1 year. Subjects will continue to receive SLC-0111 for multiple cycles of 28 days if they are receiving benefit from therapy.

Secondary Outcomes (1)

• Area under the plasma concentration versus time curve (AUC) of SLC-0111

  1 year.

Study Arms (1)

SLC-0111

EXPERIMENTAL

Drug: SLC-0111

Interventions

SLC-0111 DRUG

SLC-0111

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Males or females aged ≥ 18 years old.
• Able and willing to provide written informed consent and to comply with the study protocol and procedures.
• Histological or cytological evidence of advanced and/or metastatic or unresectable tumour(s) for which standard curative measures do not exist.
• Recovery to ≤ Grade 1 from the effects (excluding alopecia) of any prior therapy for their malignancies.
• Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
• Life expectancy greater than 3 months in the Investigator's opinion.
• The following time must have elapsed between previous therapy for cancer and first administration of SLC-0111:
• At least 4 weeks since previous cancer-directed therapy (cytotoxic agents, targeted therapy including monoclonal antibody therapy, immunotherapy, hormonal therapy, and prior radiotherapy).
• At least 4 weeks or five times the elimination half-life (whichever is shortest) of any investigational drug/biologic or combination product prior to first dose of study treatment.
• At least 3 months since prior interferon therapy.
• At least 4 weeks since any major surgery
• At least 12 weeks since any incidence of severe gastrointestinal bleeding.
• Adequate renal function:
• Creatinine ≤1.5 times upper limit of normal (ULN) or calculated creatinine clearance (CrCl) using the Cockcroft Gault formula ≥60 mL/min, or measured CrCl ≥60 mL/min.
• Adequate hepatic function:

You may not qualify if:

• Prior treatment with any drugs known to inhibit hypoxia (drugs that function under hypoxia and drugs that target cells in hypoxic regions are allowed).
• Females who are pregnant, planning to become pregnant or breastfeeding.
• Known central nervous system metastasis that is symptomatic and/or requires treatment. Radiographically stable lesions for 3 months prior to enrollment that were previously treated with steroids are permitted as long as they are not currently being treated with steroids.
• History of myocardial infarction, unstable angina, congestive heart failure (New York Heart Association class III/IV), cerebrovascular accident, transient ischaemic attack, limb claudication at rest in the 6 months prior to the first administration of SLC-0111, or ongoing symptomatic dysrhythmias, or uncontrolled atrial or ventricular arrhythmias, or uncontrolled hypertension defined as systolic blood pressure ≥150 mmHg or diastolic blood pressure ≥90 mmHg, or left ventricular ejection fraction (LVEF) \<50%.
• Any condition or illness that, in the opinion of the Investigator would compromise subject safety or interfere with the evaluation of the safety of the study drug.
• Subjects with documented cases of human immunodeficiency virus (HIV), or hepatitis B or C.
• Concurrent treatment with warfarin (Coumadin).
• Known allergy to study drug or its excipients (PEG 200, PEG 400, Soy lecithin, Vitamin E TPGS, and Propylene glycol) or severe allergy to other sulfonamides.
• Gastrointestinal condition which could interfere with the swallowing or absorption of study medication.
• Refractory nausea and vomiting, chronic gastrointestinal diseases, gastrointestinal bleeding, ulceration, or perforation within 12 weeks prior to the first administration of SLC-0111 or significant bowel resection that would preclude adequate absorption.

Sponsors & Collaborators

• Welichem Biotech Inc.: lead
• Ozmosis Research Inc.: collaborator

Study Sites (3)

Alberta Health Services - Cross Cancer Institute

Edmonton, Alberta, T6G 1Z2, Canada

Location

British Columbia Cancer Agency

Vancouver, British Columbia, V5Z 4E6, Canada

Location

Princess Margaret Cancer Centre

Toronto, Ontario, M5G 2M9, Canada

Location

MeSH Terms

Interventions

SLC-0111

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 11, 2014
• First Posted: August 13, 2014
• Study Start: October 1, 2014
• Primary Completion: March 1, 2016
• Study Completion: March 1, 2016
• Last Updated: May 17, 2016

Record last verified: 2016-05

Locations

CA (3)