A Study to Evaluate the Safety and Pharmacokinetics of CDX-0158 in Adult Patients With Advanced Solid Tumors

NCT02642016 | Completed Phase 1 FDA Drug

• 1 other identifier: CDX0158-CL-001
• Study Type: interventional
• Target: 28
• Locations: 1 country
• Sites: 4

Brief Summary

This is a dose-escalation Phase 1 study designed to determine the maximum tolerated dose (MTD) and/or recommended Phase 2 dose, and the safety profile of CDX-0158 in patients with KIT-positive advanced solid malignancies refractory to standard therapy or for which no standard therapy exists.

Conditions

Advanced Cancer

Keywords

KTN0158; Advanced Cancer; Phase 1; Monoclonal Antibody; Safety and Pharmacokinetics

Outcome Measures

Primary Outcomes (1)

• Dose limiting toxicities for CDX-0158

  Participants will be evaluated for DLTs from the first adminstration of CDX-0158 through 21 days following initial dosing.

Study Arms (1)

CDX-0158

EXPERIMENTAL

Biological: CDX-0158 (formerly known as KTN-0158)

Interventions

CDX-0158 (formerly known as KTN-0158) BIOLOGICAL

Single agent CDX-0158 until unacceptable toxicity or progressive disease

CDX-0158

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Written informed consent and any locally required authorization (eg, HIPAA) obtained from the patient/legal representative prior to performing any protocol-related procedures, including screening evaluations.
• Metastatic or unresectable cancer that expresses KIT as documented in the patient's pathology report.
• For patients with GIST, patients will have progressed on at least one prior tyrosine kinase inhibitor therapy or be intolerant. If documented to have SDH deficient or PDGFRA-D842V GIST, no prior therapy is required for study entry. Other patients with KIT positive cancers will have progressed on at least one prior therapy.
• Patients must have at least 1 lesion that is measurable using RECIST guidelines.
• Females of childbearing potential who are sexually active with a nonsterilized male partner must use 2 methods of effective contraception from screening, and must agree to continue using such precautions for 60 days after the final dose of study medication. Females of childbearing potential are defined as those who are not surgically sterile (i.e., bilateral tubal ligation, bilateral oophorectomy, or complete hysterectomy) or those who are postmenopausal (defined as 12 months with no menses without an alternative medical cause).
• Nonsterilized males who are sexually active with a female partner of childbearing potential must, with their partner, use 2 acceptable methods of effective contraception from Day 1 through 60 days after receipt of the final dose of study medication.
• ECOG status of 0 or 1.
• Adequate organ function as defined below:
• Hemoglobin ≥ 9 g/dL. This criterion must be met without transfusion.
• Absolute neutrophil count ≥ 1500/mm3
• Platelet count ≥ 100,000/mm3
• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 5 × upper limit of normal (ULN) for cases involving liver metastasis and ≤ 2.5 ×ULN for all other cases
• Bilirubin ≤ 1.5 × ULN except for cases of documented or suspected Gilbert's disease, in which bilirubin must be ≤ 5 × ULN
• Serum creatinine ≤ 1.5 g/dL

You may not qualify if:

• Receipt of anticancer therapy:
• Within 3 weeks prior to the first dose of CDX-0158 of any biologic treatment or IV chemotherapy.
• Within 2 weeks prior to the first dose of CDX-0158 of any oral therapy or 5.5 half lives whichever is longer or following palliative radiation therapy.
• Concurrent use of hormones for non-cancer related conditions (e.g., insulin for diabetes and hormone replacement therapy) is acceptable.
• Requirement for chronic immunosuppressive medication including systemic corticosteroids above the physiologic dose (30 mg/day hydrocortisone or the equivalent).
• Known allergy or past administration reaction including infusion related reaction (IRRs), anaphylactic, or anaphylactoid reactions to any component of the CDX-0158 formulation.
• History of clinically significant allergic reactions or atopic disease that may pose an increased risk of severe CDX-0158 IRRs.
• Symptomatic or untreated central nervous system metastases requiring concurrent treatment, including but not limited to surgery, radiation, and/or corticosteroids; if treated, patient must be asymptomatic for 3 months prior to study entry.
• Major surgical procedure (as defined by the investigator) within 30 days prior to Study Day 1 or incomplete recovery from any prior surgery.
• Pregnancy or breast feeding
• Uncontrolled intercurrent illness that would limit compliance with study requirements or compromise the patient such as ongoing or active infection, symptomatic congestive heart failure, hypertension requiring adjustment of medication, idiopathic and symptomatic hypotension, unstable angina pectoris, clinically significant cardiac arrhythmia including uncontrolled atrial fibrillation, active peptic ulcer disease or gastritis with ongoing blood loss, or psychiatric illness/social situations that would limit compliance or compromise the ability of the patient to give written informed consent.
• Any condition that, in the opinion of the investigator, would interfere with evaluation of the study medication or interpretation of patient safety or study results.
• Concurrent enrollment in another clinical study, unless it is an observational (non-interventional) study.
• Patients with a left ventricular cardiac ejection fraction \< 50% as assessed by an echocardiogram or MUGA scan or prolonged QTc interval of Grade 2 or higher or history of prolonged QTc interval from other drugs.

Sponsors & Collaborators

• Celldex Therapeutics: lead

Study Sites (4)

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

Location

Dana Farber Cancer Institute

Boston, Massachusetts, 02215, United States

Location

Oregon Health & Sciences University

Portland, Oregon, 97239, United States

Location

Sarah Cannon Research Institute

Nashville, Tennessee, 37203, United States

Location

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 16, 2015
• First Posted: December 30, 2015
• Study Start: December 1, 2015
• Primary Completion: January 30, 2018
• Study Completion: June 4, 2019
• Last Updated: June 12, 2019

Record last verified: 2019-06

Locations

US (4)