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Clinical Trials/NCT01581060
NCT01581060
Terminated
Phase 1

A Phase I/II, Open-label, Dose-escalation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of the MEK Inhibitor WX-554 in Patients With Solid Tumours

Heidelberg Pharma AG5 sites in 1 country41 target enrollmentMarch 2012
InterventionsWX-554
DrugsWX-554

Overview

Phase
Phase 1
Intervention
WX-554
Conditions
Advanced Solid Tumours
Sponsor
Heidelberg Pharma AG
Enrollment
41
Locations
5
Primary Endpoint
Part 1: Determination of the Optimal Biological Dose (OBD) by the assessment of ERK phosphorylation (pERK) in peripheral blood mononuclear cells (PBMC) and assessment of TNF-alpha in plasma.
Status
Terminated
Last Updated
11 years ago

Overview

Brief Summary

The aim of part 1 of this study is to determine the optimal biological dose (OBD) and maximum tolerated dose (MTD) for WX-554 and the recommended dose/dose schedules for the chronic treatment in part 2. The aim of part 2 is to further determine the safety and tolerability of chronic treatment with WX-554.

Registry
clinicaltrials.gov
Start Date
March 2012
End Date
April 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with advanced, metastatic and/or progressive solid tumours for whom there is no effective standard therapy available.
  • Evaluable or measurable disease
  • Has normal organ functions; is no greater than 2 on the ECOG Performance Scale
  • life expectancy of \>3 months
  • negative hCG test in women of childbearing potential

Exclusion Criteria

  • Patients who received an investigational anti-cancer drug within 4 weeks of starting the study
  • Patients who received major surgery, radiotherapy, or immunotherapy within 4 weeks of starting the study
  • Clinically significant, unresolved toxicity from previous anti-cancer therapy Patients
  • Patients who previously received a MEK inhibitor
  • Presence of active gastrointestinal disease or other condition that will interfere significantly with the absorption, distribution, metabolism, or excretion of drugs.
  • Known medical history of retinal vein occlusion, intraocular pressure greater than 21 mm Hg or patient considered at risk of retinal vein thrombosis.
  • Known HIV positivity or active hepatitis B or C infection.
  • History of clinically significant cardiac condition

Arms & Interventions

WX-554

Intervention: WX-554

Outcomes

Primary Outcomes

Part 1: Determination of the Optimal Biological Dose (OBD) by the assessment of ERK phosphorylation (pERK) in peripheral blood mononuclear cells (PBMC) and assessment of TNF-alpha in plasma.

Time Frame: Cycle 1 (21 days)

Part 1: Determination of the Maximum Tolerated Dose (MTD) for WX-554 by the evaluation of DLTs in 3-6 patients at the end of 1 treatment cycle

Time Frame: Cycle 1 (21 days)

Part 2: To further determine the safety and tolerability by evaluating the incidence and severity of adverse events and serious adverse events (as per CTCAE grading), changes in hematology and chemistry values, vital signs, ECGs.

Time Frame: expected average of 3-6 months

Secondary Outcomes

  • Assessment of PK variables maximum observed concentration (Cmax), minimum observed concentration (Cmin), time at which Cmax was present (tmax), Area Under Curve (AUC)(PK profile on day 1 and day 8)
  • Assessment of ERK phosphorylation (pERK) in PBMC and tissue, assessment of TNF-alpha in plasma after oral intake of the OBD/MTD.(expected average of 3-6 months)
  • Tumour response evaluation using RECIST 1.1(expected average of 3-6 months)

Study Sites (5)

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