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Clinical Trials/NCT04511845
NCT04511845
Active, not recruiting
Phase 1

A Phase I, Open-Label, Multicenter, Dose Escalation and Cohort Expansion Study of SPYK04 as Monotherapy in Patients With Locally Advanced or Metastatic Solid Tumors

Chugai Pharmaceutical15 sites in 2 countries113 target enrollmentSeptember 10, 2020

Overview

Phase
Phase 1
Intervention
SPYK04
Conditions
Locally Advanced or Metastatic Solid Tumors
Sponsor
Chugai Pharmaceutical
Enrollment
113
Locations
15
Primary Endpoint
Safety and tolerability of SPYK04 (Dose limiting toxicities) [Dose escalation]
Status
Active, not recruiting
Last Updated
9 months ago

Overview

Brief Summary

Phase I, open-label, multi-center study

Registry
clinicaltrials.gov
Start Date
September 10, 2020
End Date
September 30, 2026
Last Updated
9 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • (Both Part I and Part II)
  • Age \>= 18 years at time of signing informed consent form
  • ECOG performance status of 0 or 1
  • Patients with a locally advanced, recurrent, or metastatic solid tumor for which standard therapy either does not exist or has proven ineffective or intolerable
  • (Part I only)
  • Patients with measurable and/or evaluable disease per RECIST v1.1
  • Patients with MAPK pathway alterations positive solid tumor (i.e., BRAF, K/N/H-RAS mutations)
  • (Part II only)
  • Patients with measurable disease per RECIST v1.1
  • Patients with KRAS mutated NSCLC (NSCLC cohort)

Exclusion Criteria

  • (Both Part I and Part II)
  • Significant cardiovascular disease, such as New York Heart Association (NYHA) cardiac disease (Class II or greater), unstable angina, or myocardial infarction within the previous 6 months or unstable arrhythmias within the previous 3 months
  • Patients with primary central nervous system (CNS) malignancy, untreated CNS metastases requiring any anti-tumor treatment, or active CNS metastases
  • Patients with current severe, uncontrolled systemic disease (including, but not limited to, clinically significant cardiovascular disease, pulmonary disease, or renal disease, ongoing or active infection)
  • Patients with a history or complication of interstitial lung disease (ILD)

Arms & Interventions

Expansion part in NSCLC, ovarian cancer and other solid tumors

Patients will receive SPYK04 at the recommended dose.

Intervention: SPYK04

Dose escalation cohort of SPYK04

Patients will receive SPYK04 at escalated dose.

Intervention: SPYK04

Outcomes

Primary Outcomes

Safety and tolerability of SPYK04 (Dose limiting toxicities) [Dose escalation]

Time Frame: From first dose until the end of Cycle 1 (approximately 35 days)

Incidence and nature of DLTs

Safety and tolerability of SPYK04 (Electrocardiograms in triplicate) [Dose escalation]

Time Frame: From first dose until the end of Cycle 1 (approximately 35 days)

Heart Rate

Preliminary anti-tumor activity of SPYK04 [Cohort expansion]

Time Frame: From screening until disease progression, study discontinuation, withdrawal or death, whichever occurs first, assessed up to 42 months (study completion)

Objective Response Rate (ORR) is defined as proportion of patients who had a confirmed complete response (CR) or partial response (PR), as determined by the investigator with use of Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1)

Safety and tolerability of SPYK04 (Adverse Events) [Dose escalation]

Time Frame: From Cycle 0 Day 1 until 28 days after the last dose of study treatment, assessed up to 42 months (study completion)

Incidence, nature, and severity of adverse events (AEs) as assessed by the NCI CTCAE v5.0

Pharmacokinetics of SPYK04 [Dose escalation]

Time Frame: From Cycle 0 Day 1 until 28 days after the last dose of study treatment, assessed up to 42 months (study completion)

Area under the concentration versus time curve (AUC) of SPYK04

Secondary Outcomes

  • Safety and tolerability of SPYK04 (AEs) [Cohort expansion](From Cycle 1 Day 1 until 28 days after the last dose of study treatment, assessed up to 42 months (study completion))
  • Preliminary anti-tumor activity of SPYK04 [Dose escalation](From screening until disease progression, study discontinuation, withdrawal or death, whichever occurs first, assessed up to 42 months (study completion))
  • Preliminary anti-tumor activity of SPYK04 [Cohort expansion](From screening until disease progression, study discontinuation, withdrawal or death, whichever occurs first, assessed up to 42 months (study completion))
  • Pharmacokinetics of SPYK04 [Cohort expansion](From Cycle 1 Day 1 until 28 days after the last dose of study treatment, assessed up to 42 months (study completion))
  • Pharmacodynamics of SPYK04 [Cohort expansion](From screening until the time of partial response or stable disease lasting for more than 4 months, and the time of progressive disease, if possible, an average of 1 year)

Study Sites (15)

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