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Clinical Trials/NCT04686383
NCT04686383
Completed
Phase 1

A Phase I, Multi-center, Open-label, Dose-escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of CAL056 Mesylate in Patients With Solid Tumors Resistant or Refractory to Standard Treatments

Calgent Biotechnology Co., Ltd3 sites in 2 countries17 target enrollmentDecember 29, 2020

Overview

Phase
Phase 1
Intervention
CAL056 mesylate
Conditions
Resistant or Refractory Solid Tumors
Sponsor
Calgent Biotechnology Co., Ltd
Enrollment
17
Locations
3
Primary Endpoint
Number of patients with adverse events (AEs), serious adverse events (SAEs), and treatment emergent adverse events (TEAEs)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This is a multi-center, open-label, dose-escalation, phase I study to evaluate the safety, tolerability, pharmacokinetics (PK), preliminary efficacy, and pharmacodynamics of CAL056 mesylate in cancer patients with resistant or refractory solid tumors.

Detailed Description

Patients with resistant or refractory malignant solid tumors and no standard treatment available will be screened for the eligibility. Patients will be screened within 28 days prior to the first dose of CAL056 mesylate. Eligible patients will receive CAL056 mesylate daily with the assigned dose level for 28 days (Day 1 to Day 28) for each treatment cycle. Patients will be administered with CAL056 mesylate at clinical site at scheduled visits (i.e. Day 1/Visit 1, Day 8/Visit 2, Day 15/ Visit 3, Day 22/Visit 4, Day 28/Visit 5). Remaining doses of CAL056 mesylate on all other days will be self-administered by patients at home. After the administration of CAL056 mesylate on Day 1 and Day 28, patients can stay at the clinical site for 24 hours to have safety monitoring and blood samples collected for PK analysis. Only patients completing Cycle 1 without a dose-limiting toxicity (DLT) or disease progression will be allowed to continue the subsequent cycles at the same dose level. The maximum number of dosing cycle is 6 cycles in each patient in this study. Continuation of using CAL056 mesylate may be permitted after the evaluation of the risk/benefit in individual patient by the Investigators and with the approval of Calgent. During the Cycle 1 of study period, a total of 5 visits are scheduled to evaluate the safety, PK, preliminary efficacy, and pharmacodynamics of CAL056 mesylate. Each visit is planned on Day 1 of each subsequent cycle if patients continue the treatment of CAL056 mesylate. After the end treatment of CAL056 mesylate, an end of treatment (EOT) visit and a safety follow-up visit will be scheduled.

Registry
clinicaltrials.gov
Start Date
December 29, 2020
End Date
June 30, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with age ≥ 18 years old
  • Patients with resistant or refractory solid tumors confirmed by histology which are unresponsive to standard therapies
  • Patients with at least one measurable lesion per RECIST version 1.
  • Patients with Eastern Cooperative Oncology Group performance status (ECOG-PS) ≤ 2
  • Patients with at least 3 months of life expectancy as judged by the investigators
  • Patients with adequate bone marrow reserve and organ function
  • Patients with the negative result for testing Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)
  • Female patients are eligible to participate if they are of non-childbearing potential or have documentation of a negative serum pregnancy test at screening. Sexually active pre-menopausal women of childbearing potential must agree to use adequate, highly effective contraceptive measures during and upon completion of the study and for at least 6 months after the last dose of study drug
  • Male patients who agree to use an adequate method of contraception during and upon completion of the study and for at least 6 months after the last dose of study drug
  • Patients must be willing and be able to provide written informed consent for the study.

Exclusion Criteria

  • History of other invasive malignancy that is currently active and/or has been treated within 12 months prior to screening
  • Patients with the presence of symptomatic central nervous system (CNS) metastases requiring radiation treatment, surgery, or continuous use of corticosteroids or patients with untreated or developing brain metastasis causing any symptoms, such as neurologic deficits, seizures, or headache
  • Any prior adjuvant cytotoxic chemotherapy within 4 weeks prior to screening
  • Any radiotherapy within 2 weeks prior to screening
  • Pre-existing chemotherapy-related peripheral neuropathy
  • Currently participating or has participated in a study of an investigational product within 4 weeks prior to the first dose of CAL056 mesylate
  • Patients with history of organ or stem cell transplant requiring immunosuppressive medications
  • Active autoimmune disease
  • Pulmonary conditions such as sarcoidosis, silicosis, idiopathic pulmonary fibrosis, or hypersensitivity pneumonitis
  • Patients who have chronic obstructive pulmonary disease (COPD) or asthma

Arms & Interventions

Cohort 1: 20 mg CAL056 mesylate

Patients will receive oral dose of 20 mg CAL056 mesylate once daily under fasting condition in the morning for 28 days during each cycle.

Intervention: CAL056 mesylate

Cohort 2: 40 mg CAL056 mesylate

Patients will receive oral dose of 40 mg CAL056 mesylate once daily under fasting condition in the morning for 28 days during each cycle.

Intervention: CAL056 mesylate

Cohort 3: 80 mg CAL056 mesylate

Patients will receive oral dose of 80 mg CAL056 mesylate once daily under fasting condition in the morning for 28 days during each cycle.

Intervention: CAL056 mesylate

Cohort 4: 120 mg CAL056 mesylate

Patients will receive oral dose of 120 mg CAL056 mesylate once daily under fasting condition in the morning for 28 days during each cycle.

Intervention: CAL056 mesylate

Cohort 5: 160 mg CAL056 mesylate

Patients will receive oral dose of 160 mg CAL056 mesylate once daily under fasting condition in the morning for 28 days during each cycle.

Intervention: CAL056 mesylate

Outcomes

Primary Outcomes

Number of patients with adverse events (AEs), serious adverse events (SAEs), and treatment emergent adverse events (TEAEs)

Time Frame: From screening visit until safety follow-up visit (at 28 days after the EOT) or before starting new anticancer treatment, whichever comes first (up to 1-year)

To evaluate the safety and tolerability of CAL056 mesylate in cancer patients.

Number of patients with AEs qualified as dose-limiting toxicities (DLTs)

Time Frame: Cycle 1 (28 days)

Dose-limiting toxicities are evaluated using National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.

Determination of tolerability and maximum tolerated dose (MTD) of CAL056 mesylate by DLTs using NCI CTCAE version 5.0

Time Frame: Cycle 1 (28 days)

MTD will be the highest dose associated with occurrence of DLTs ≤ 33% (e.g. 2/6 evaluable patients experience a DLT during the first treatment Cycle).

Evaluation of the PK profile of CAL056 mesylate: Maximum observed concentration (Cmax)

Time Frame: At Day 1 and Day 28 of Cycle 1, at Day 1 of subsequent cycles until Cycle 6 (except for Cycle 2) (each cycle is 28 days in length)

Pharmacokinetics profile will be evaluated following a comprehensive PK parameter, such as Cmax.

Evaluation of the PK profile of CAL056 mesylate: Area under the concentration-time curve (AUC)

Time Frame: At Day 1 and Day 28 of Cycle 1, at Day 1 of subsequent cycles until Cycle 6 (except for Cycle 2) (each cycle is 28 days in length)

Pharmacokinetics profile will be evaluated following a comprehensive PK parameter, AUC.

Evaluation of the PK profile of CAL056 mesylate: Time to reach Cmax (Tmax)

Time Frame: At Day 1 and Day 28 of Cycle 1, at Day 1 of subsequent cycles until Cycle 6 (except for Cycle 2) (each cycle is 28 days in length)

Pharmacokinetics profile will be evaluated following comprehensive PK parameter, such as Tmax.

Evaluation of the PK profile of CAL056 mesylate: Apparent terminal elimination half-life (t½)

Time Frame: At Day 1 and Day 28 of Cycle 1, at Day 1 of subsequent cycles until Cycle 6 (except for Cycle 2) (each cycle is 28 days in length)

Pharmacokinetics profile will be evaluated following comprehensive PK parameter, such as t½.

Preliminary determination of the recommended phase II dose (RP2D) of CAL056 mesylate

Time Frame: Cycle 1 (28 days)

The RP2D will be preliminarily determined by the PK profile, type and severity of drug related toxicity, clinical suitability for long-term administration.

Secondary Outcomes

  • Evaluation of the preliminary efficacy of CAL056 mesylate in tumor response as assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1(At the screening visit and within 7 days prior to Day 1 of odd cycles (i.e., Cycle 3 and Cycle 5) (each cycle is 28 days in length) and at EOT/Early Termination (ET) (up to 21 months))

Study Sites (3)

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