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Safety Study of SLC-391 in Subjects With Solid Tumors

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ClinicalTrials.gov Identifier: NCT03990454
Recruitment Status : Recruiting
First Posted : June 19, 2019
Last Update Posted : October 30, 2019
Sponsor:
Information provided by (Responsible Party):
SignalChem Lifesciences Corporation

Brief Summary:

SLC-391 is a novel, potent and specific small molecule inhibitor of receptor tyrosine kinase AXL with desirable potency and pharmaceutical properties. It has demonstrated antiproliferative activity against different tumour cell lines in vitro and efficacy in different animal models including nonsmall cell lung cancer (NSCLC), chronic myeloid leukemia (CML) and (acute myeloid leukemia (AML) models. It has also exhibited strong synergy with other approved targeted therapies in different animal models.

This is the first clinical study with SLC-391. The goals of this study are to evaluate the safety, pharmacokinetic (PK), and pharmacodynamic profile of SLC-391, and then to identify a safe and pharmacologically active dose for evaluation in subsequent cohorts or clinical studies. In addition, change from baseline of possible blood biomarkers (soluble AXL and Gas 6) may be evaluated.

This is an open-label, multicentre, phase 1, dose-escalation, dose-expansion, first in human study to evaluate the safety of SLC-391 administered orally (once-daily) in 21-day cycles to subjects with advanced solid tumours.


Condition or disease Intervention/treatment Phase
Solid Tumor Drug: SLC-391 Phase 1

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 50 participants
Intervention Model: Sequential Assignment
Intervention Model Description:

The study will employ a 3+3 dose-escalation design. Cohorts (same dose level) of 3 to 6 evaluable subjects will participate in a dose-escalation scheme in which the dose of SLC-391 will be increased in each consecutive cohort. Evaluation of a cohort of ≥ 3 subjects that have completed a 21-day cycle (cycle 1) is required prior to defining a new SLC-391 dose and schedule for the next cohort. Dose-escalation decisions by the Data Review Committee will take into account all available data including PK/pharmacodynamic data and the safety profile of prior cohorts. Based on all available emerging data, alternative dosing schedules, frequency, or dose reductions may be considered.

Subjects with certain tumour types (eg, nonsmall cell lung cancer, ovarian) may be enrolled in expansion cohorts (≤ 12 subjects) at doses less than or equal to Maximum Tolerated Dose (MTD) in order to better characterise the antitumour activity and safety of SLC-391 and to define the Recommended Phase 2 Dose dose.

Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1, Open-label, Dose-escalation, and Dose-expansion Study of the Safety and Pharmacokinetics of the AXL Inhibitor SLC-391 Administered Orally to Subjects With Solid Tumours
Actual Study Start Date : September 17, 2019
Estimated Primary Completion Date : August 1, 2020
Estimated Study Completion Date : August 1, 2020

Arm Intervention/treatment
Experimental: Dose escalation/expansion

The starting dose will be 25 mg/day and subsequent doses will be determined after an internal review by Data Review Committee of all available safety, PK and PD data from the minimum required number of subjects who complete cycle 1. All dose-escalation decisions and the rationale for progressing to the next cohort will be documented.

A subject may continue treatment with SLC-391 in 21-day cycles until the treatment discontinuation criteria are met.

Subjects with certain tumour types (e.g., NSCLC or ovarian) may be enrolled in expansion cohorts of up to 12 subjects at doses less than or equal to the MTD to better characterise the activity and safety of SLC-391 and define the Recommended Phase 2 Dose (RP2D) dose.

Drug: SLC-391
SLC-391 is an AXL inhibitor




Primary Outcome Measures :
  1. Number of Participants with Adverse Events (AEs) as assessed by NCI-CTCAE v5.0 [ Time Frame: 2 years ]
    To assess AEs as criteria of safety of oral SLC-391

  2. Maximum Tolerated Dose of SLC-391 [ Time Frame: 21 days ]
    To determine the maximum tolerated dose (MTD) of SLC-391


Secondary Outcome Measures :
  1. Area under the plasma concentration versus time curve (AUC) of SLC-391 [ Time Frame: Day 1 predose through to Day 21 post-final dose ]
    Changes in AUC over time in subjects taking SLC-391 once daily.

  2. Maximum Observed Plasma Concentration (Cmax) [ Time Frame: Day 1 predose through to Day 21 post-final dose ]
    Cmax is the maximum observed plasma concentration in ng/mL

  3. Time to the Maximum Observed Plasma Concentration (Tmax) [ Time Frame: Day 1 predose through to Day 21 post-final dose ]
    Tmax is the time in hours to reach Cmax following dosing

  4. Terminal elimination half-life (t1/2) [ Time Frame: Day 1 predose through to Day 21 post-final dose ]
    The time in hours required for the plasma level of the study drug to decrease by one-half during the terminal elimination phase

  5. Recommended Dose of SLC-391 for future trials [ Time Frame: 2 years ]
    Determine the recommended phase 2 dose (RP2D) of SLC-391

  6. Preliminary efficacy of SLC-391 [ Time Frame: 2 years ]
    Determine tumour response defined by the Response Evaluation Criteria in Solid Tumours (RECIST) 1.1 to SLC-391



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Be 18 years of age or older at the time of signing the informed consent.
  • Have a histologically or cytologically confirmed diagnosis of a solid tumour malignancy that is advanced and/or metastatic or unresectable and for which standard or curative measures do not exist or are no longer effective.
  • Have measurable disease as per the Response Evaluation Criteria in Solid Tumours (RECIST) 1.1.
  • Have a performance status score of 0 or 1 according to the Eastern Cooperative Oncology Group (ECOG) scale.
  • Be able to ingest oral medication.
  • Have adequate organ function,
  • Have recovered to ≤ grade 1 from the effects of any prior cancer therapy, except for alopecia; irreversible neuropathy should have recovered to ≤ grade 2. Toxic effects also include laboratory test abnormalities.
  • Be afebrile at baseline prior to SLC-391 administration (ie, < 38.0 °C).
  • Have a life expectancy greater than 3 months, in the Investigator's opinion.
  • The following time must have elapsed between previous therapy for cancer and first dose of SLC-391:

    1. At least 4 weeks since previous cancer-directed therapy, including investigational agents or devices (cytotoxic agents, targeted therapy including monoclonal antibodies, immunotherapy, hormonal therapy, and prior radiotherapy) with the exception of nitrosoureas/mitomycin where 6 weeks since these therapies.
    2. At least 4 weeks or 5 times the elimination half-life (whichever is shortest) of any investigational agents, including drugs, biologics, or combination products.
    3. At least 4 weeks since any major surgery.
  • 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 3 months after the last dose of study drug. Male subjects must also agree to refrain from donating sperm for the duration of the study, including during dose interruptions and for 3 months after the last dose administered.
  • Be able and willing to provide signed informed consent and comply with the requirements, assessment schedule, dosing schedule, and restrictions listed in the informed consent form (ICF) and study protocol.

Exclusion Criteria:

  • Prior use of any AXL inhibitor
  • Localised or metastatic prostate cancer subjects who are concurrently receiving anti-cancer hormonal therapy.
  • Refractory nausea and vomiting, chronic gastrointestinal (GI) diseases, GI bleeding, ulceration, or perforation within 12 weeks prior to the first dose of the study drug, or significant bowel resection that would preclude adequate absorption, distribution, metabolism, or excretion of the study drug.
  • 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, stroke or subarachnoid hemorrhage, coagulopathy, deep vein thrombosis, pulmonary embolism in the 6 months prior to consent.
  • Uncontrolled hypertension (≥ 160/100 mmHg).
  • History of or ongoing symptomatic dysrhythmias, uncontrolled atrial or ventricular arrhythmias, or heart block (excluding 1st degree block, consisting of PR interval prolongation only). Controlled atrial fibrillation is allowed.
  • QTcF interval > 480 msec.
  • Severe respiratory illness requiring supplemental oxygen or that significantly impacts functional status in daily life including a known history of active tuberculosis (Mycobacterium tuberculosis).
  • History of significant weight loss (≥ 7 kgs/15 lbs) within 4 weeks prior to the first dose of study drug.
  • Immunocompromised or those with known autoimmune conditions, known human immunodeficiency virus (HIV), or known active hepatitis (according to diagnostic serology results that are positive for active hepatitis B [HBV; including core antibody and surface antigen; AntiHBc and HBsAg, respectively] or hepatitis C [HCV] infection). Note: If any serology is positive, qualitative polymerase chain reaction will be obtained and results must be negative for eligibility.
  • Active uncontrolled infection, or an unstable or severe intercurrent medical condition that requires treatment.
  • History of solid organ transplant or bone marrow transplant.
  • 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 and jeopardises compliance with the protocol and study visits.
  • Brain metastases and central nervous system disease including leptomeningeal disease.
  • History of prior malignancy, except for the following: curatively treated basal or squamous cell carcinoma of the skin (nonmelanoma skin cancer); cervical or vaginal intra-epithelial neoplasia; or noninvasive breast cancer in situ at screening. Subjects with other curatively treated malignancies who have had no evidence of metastatic disease and a > 2-year disease-free interval may be enrolled after approval by the Medical Monitor or SignalChem Lifesciences (SLC) designee.
  • Females who are pregnant, planning to become pregnant, or breastfeeding.
  • Hypersensitivity to the study drug or excipients (lactose, microcrystalline cellulose, magnesium stearate, and gelatin capsule shell).

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03990454


Contacts
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Contact: Zaihui Zhang, PhD 1-604-232-4600 ext 114 zzhang@signalchemcorp.com
Contact: Madhu Singh, PhD 1-604-899-9269 msingh@signalchemcorp.com

Locations
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Canada, Ontario
Juravinski Cancer Centre Not yet recruiting
Hamilton, Ontario, Canada, L8V 5C2
Contact: Yvonne Kirndale         
Principal Investigator: Sebastien Hotte, MD         
The Ottawa Hospital Cancer Center Recruiting
Ottawa, Ontario, Canada, K1H 8L6
Contact: Lena McAleer         
Principal Investigator: Scott Laurie, MD         
Princess Margaret Cancer Centre Recruiting
Toronto, Ontario, Canada, M5G 2M9
Contact: Tuhina Paul         
Principal Investigator: Natasha Leighl, MD         
Sponsors and Collaborators
SignalChem Lifesciences Corporation
Investigators
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Study Director: Zaihui Zhang, PhD SignalChem Lifesciences Corporation

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Responsible Party: SignalChem Lifesciences Corporation
ClinicalTrials.gov Identifier: NCT03990454     History of Changes
Other Study ID Numbers: SLC-391-101
First Posted: June 19, 2019    Key Record Dates
Last Update Posted: October 30, 2019
Last Verified: October 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by SignalChem Lifesciences Corporation:
AXL Inhibitor
Solid Tumor
Additional relevant MeSH terms:
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Neoplasms