Study of IMC-3G3 in Patients With Tumors That Are Not Responding to Standard Therapies or No Therapy is Available
Phase I Study of Anti-Platelet Derived Growth Factor Receptor Alpha (PDGFRa) Monoclonal Antibody IMC-3G3 in Patients With Advanced Solid Tumors Who No Longer Respond to Standard Therapy or for Whom no Standard Therapy is Available
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Locations
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Indiana
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Indianapolis, Indiana, United States, 46282
- ImClone Investigational Site
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Texas
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Houston, Texas, United States, 77030
- ImClone Investigational Site
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Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Histopathological-documented, measurable, or non measurable, advanced primary tumor or recurrent solid tumor or lymphoma unresponsive to standard therapy or for which there is no standard therapy available.
- Eastern Cooperative Oncology Group (ECOG) performance status score of ≤ 2 at study entry.
- Able to provide written informed consent.
- Age 18 years or older.
- Life expectancy of > 3 months.
- Adequate hematologic function, as defined by: an absolute neutrophil count ≥ 1500/mm3; a platelet count ≥ 100,000/mm3
- Adequate hepatic function, as defined by: a total bilirubin level ≤ 1.5 x the upper limit of normal (ULN); aspartate transaminase (AST) and alanine transaminase (ALT) levels ≤ 2.5 x the ULN or ≤ 5 x the ULN if known liver metastases
- Adequate renal function, as defined by serum creatinine level ≤ 1.5 x the ULN.
- Uses effective contraception (per the institutional standard), if procreative potential exists.
- Adequate recovery from recent surgery, chemotherapy, and radiation therapy.
- Accessible for treatment and follow-up, must be treated at the participating center.
Exclusion Criteria:
- Received chemotherapy or therapeutic radiotherapy 28 days prior to the first dose of study medication or has ongoing side effects ≥ grade 2 due to agents administered more than 28 days earlier.
- Uncontrolled intercurrent illness including, but not limited to: ongoing or active infection requiring parenteral antibiotics; symptomatic congestive heart failure; unstable angina pectoris, angioplasty, stenting, or myocardial infarction 6 months prior to the first dose of study medication; uncontrolled hypertension; clinically significant cardiac arrhythmia including but not limited to: multifocal premature ventricular contractions, bigeminy, trigeminy, ventricular tachycardia that is symptomatic or requires treatment or asymptomatic sustained ventricular tachycardia; uncontrolled diabetes; psychiatric illness/social situations that would compromise patient safety or limit compliance with study requirements
- Progressive or symptomatic brain metastases
- Has a serious or nonhealing active wound, ulcer, or bone fracture.
- Known human immunodeficiency virus positivity.
- Major surgical procedure, an open biopsy, or a significant traumatic injury 28 days prior to treatment.
- Is currently or has recently used (28 days prior to) a thrombolytic agent.
- Currently using full-dose warfarin (an exception is low-dose warfarin to maintain patency of pre-existing, permanent, indwelling intravenous [I.V.] catheters; for patients receiving warfarin, the international normalized ratio [INR] should be < 1.5). A patient requiring heparin is excluded.
- Undergoes chronic daily treatment with aspirin (> 325 mg/day) or nonsteroidal anti-inflammatory medications known to inhibit platelet function (cyclooxygenase-2 [COX-2] inhibitors are permitted).
- Has a history or clinical evidence of a deep venous or arterial thrombosis (including pulmonary embolism) 6 months prior to the first dose of study medication.
- Has proteinuria ≥ 2+ by routine urinalysis
- Pregnancy (confirmed by serum beta human chorionic gonadotropin) or lactating
- Received prior treatment with agents targeting the PDGFR ligand or receptor 6 weeks prior to the first dose of study medication.
- Received prior treatment with monoclonal antibodies 6 weeks prior to the first dose of study medication.
- Has a history of allergic reactions to monoclonal antibodies or other therapeutic proteins.
Study Plan
How is the study designed?
Design Details
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
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Experimental: IMC-3G3
All patients will receive intravenous infusions of IMC-3G3, with the dose depending on which cohort they are enrolled into.
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Intravenously, once every week for Cohorts 1 through 3 and once every other week for Cohorts 4 and 5. Starting dose will be 4mg/kg in Cohort 1, with dose doubling between cohorts.
Dose escalation of 100% (2 x previous dose) Dose escalation increment reduced to 33% (1.33 x previous dose).
Cohorts 4 and 5 will receive 15mg/kg and 20mg/kg, intravenously, once every other week.
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What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Summary of Participants Reporting Adverse Events
Time Frame: Approximately 36 months
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Approximately 36 months
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|
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Maximum Tolerated Dose (MTD)
Time Frame: Approximately 36 months
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After all patients complete a cohort, toxicity data is reviewed before the next cohort of patients is treated at the next higher dose level
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Approximately 36 months
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Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Pharmacokinetics
Time Frame: 6 weeks
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6 weeks
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Anti-IMC-3G3 Antibody Assessment
Time Frame: Approximately 36 months
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Approximately 36 months
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Antitumor Activity of IMC-3G3 as Monotherapy
Time Frame: 6 weeks
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6 weeks
|
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Pharmacodynamics
Time Frame: 6 weeks
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6 weeks
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Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Study Director: E-mail: ClinicalTrials@ ImClone.com, Eli Lilly and Company
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- 13937
- CP15-0601 (Other Identifier: ImClone, LLC)
- I5B-IE-JGDC (Other Identifier: Eli Lilly and Company)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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