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

Solid Tumours Clinical Trial

Official title:

A Phase I, Multi-center, Open-label, Study to Investigate the Safety, Tolerability and Pharmacokinetic of SLC-0111 in Subjects With Advanced Solid Tumours

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02215850
• Other study ID #: OZM-055/SLC0111-14-C01
• Status: Recruiting
• Phase: Phase 1
• First received: August 11, 2014
• Last updated: December 17, 2015
• Start date: October 2014
• Est. completion date: April 2016

Study information

• Verified date: December 2015
• Source: Welichem Biotech Inc.
• Contact: Ben Boyd
• Phone: 416-673-8436
• Email: ben.boyd[@]ozmosisresearch.ca
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 24
• Est. completion date: April 2016
• Est. primary completion date: February 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Males or females aged = 18 years old.

2. Able and willing to provide written informed consent and to comply with the study protocol and procedures.

3. Histological or cytological evidence of advanced and/or metastatic or unresectable tumour(s) for which standard curative measures do not exist.

4. Recovery to = Grade 1 from the effects (excluding alopecia) of any prior therapy for their malignancies.

5. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1

6. Life expectancy greater than 3 months in the Investigator's opinion.

7. 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.

8. 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.

9. Adequate hepatic function:

• Serum bilirubin =1.5 times upper limit of normal (ULN)

• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =2.5 x ULN (=5 x ULN if liver lesions present [i.e. liver metastasis or primary tumour of the liver for hepatocellular carcinoma (HCC]).

10. Adequate bone marrow function:

• Absolute neutrophil count =1.5 x 109/L

• Platelets =100 x 109/L

• Haemoglobin =90 g/L

11. Adequate coagulation tests: international normalised ratio (INR) =1.5 x ULN.

12. Corrected QT interval (QTcB) < 470 ms

13. Ability to take oral liquid medication

14. Negative urine pregnancy test within 14 days prior to the first dose of study therapy for women of child-bearing potential, defined as a sexually mature woman who has not undergone a hysterectomy/oophorectomy or who has not been naturally postmenopausal for at least 24 consecutive months (i.e., who has had menses any time in the preceding 24 consecutive months).

15. Sexually-active women of child-bearing potential and sexually-active male subjects with a female partner of child-bearing potential or pregnant must agree to use acceptable double-barrier methods of contraception to avoid pregnancy from screening, for the duration of the study, and for 4 months after the last dose of study drug (Rhythm methods and/or abstinence will not be considered as highly effective methods of birth control).

16. Subjects must agree not to donate gametes (i.e. sperms and eggs) during the study and for 4 months following their last dose of SLC-0111.

Exclusion Criteria:

1. Prior treatment with any drugs known to inhibit hypoxia (drugs that function under hypoxia and drugs that target cells in hypoxic regions are allowed).

2. Females who are pregnant, planning to become pregnant or breastfeeding.

3. 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.

4. 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%.

5. 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.

6. Subjects with documented cases of human immunodeficiency virus (HIV), or hepatitis B or C.

7. Concurrent treatment with warfarin (Coumadin).

8. 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.

9. Gastrointestinal condition which could interfere with the swallowing or absorption of study medication.

10. 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.

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Solid Tumours

Intervention

Drug:
• SLC-0111

Locations

Country	Name	City	State
Canada	Alberta Health Services - Cross Cancer Institute	Edmonton	Alberta
Canada	Princess Margaret Cancer Centre	Toronto	Ontario
Canada	British Columbia Cancer Agency	Vancouver	British Columbia

Sponsors (2)

Lead Sponsor	Collaborator
Welichem Biotech Inc.	Ozmosis Research Inc.

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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.	Yes
Secondary	Area under the plasma concentration versus time curve (AUC) of SLC-0111	Changes in AUC over time in subjects taking SLC-0111 once daily.	1 year.	No