A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of KTN3379 in Adult Subjects With Advanced Tumors
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT02014909 |
Recruitment Status :
Completed
First Posted : December 18, 2013
Last Update Posted : July 24, 2017
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Advanced Cancer | Biological: KTN3379 | Phase 1 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 64 participants |
Allocation: | Non-Randomized |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Part I and Part II A Phase 1 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of KTN3379 in Adult Subjects With Advanced Tumors Alone or With Chemotherapy |
Study Start Date : | January 2014 |
Actual Primary Completion Date : | May 25, 2017 |
Actual Study Completion Date : | June 5, 2017 |
Arm | Intervention/treatment |
---|---|
Experimental: KTN3379
KTN3379
|
Biological: KTN3379
Single agent KTN3379 or in combination administered until unacceptable toxicity or progressive disease |
Experimental: Part II, Arm A
Combination of KTN3379 and cetuximab
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Biological: KTN3379
Single agent KTN3379 or in combination administered until unacceptable toxicity or progressive disease |
Experimental: Part II, Arm B
Combination of KTN3379 and erlotinib
|
Biological: KTN3379
Single agent KTN3379 or in combination administered until unacceptable toxicity or progressive disease |
Experimental: Part II, Arm C
Combination of KTN3379 and vemurafenib
|
Biological: KTN3379
Single agent KTN3379 or in combination administered until unacceptable toxicity or progressive disease |
Experimental: Part II, Arm D
Combination of KTN3379 and trastuzumab
|
Biological: KTN3379
Single agent KTN3379 or in combination administered until unacceptable toxicity or progressive disease |
- Dose limiting toxicities for KTN3379 alone or in combination [ Time Frame: Participants will be followed for the duration of treatment, an expected average of 3 cycles/9 weeks ]Continued assessment of safety
- Area Under the Concentration-Time Curve (AUC 0 through end of study) [ Time Frame: Prior to the initial dose on day 1 through duration of treatment, an expected average of 3 cycles/9 weeks ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Major Inclusion Criteria:
- Part I Histologically- or cytologically-confirmed advanced solid tumors that are refractory to standard therapy or for which no standard therapy exist. Part II Arm A have head and neck cancer or K-Ras wild type EGFR expressing colon cancer, Arm B, have non small cell lung cancer, Arm C, have BRAF V600E mutated melanoma and Arm D have HER2 positive breast or gastric cancer that has progressed following one or more treatments for advanced or metastatic disease.
- Eastern Cooperative Oncology Group (ECOG) status of 0 or 1
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Adequate organ function as defined below:
- Hemoglobin ≥ 9 g/dL
- Absolute neutrophil count ≥ 1500/mm3
- Platelet count ≥ 100,000/mm3
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 5 × institutional 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
- Measurable disease by RECIST
- Females must be surgically sterile, one year post menopausal or negative results for a pregnancy test performed at Screening and agree to use two methods of contraception; Males who have not had a vasectomy must agree to two methods of contraception
Major Exclusion Criteria:
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Receipt of anticancer therapy:
- within 3 weeks prior to the first dose of KTN3379, or
- within 6 weeks or 7 half lives prior to the first dose of KTN3379 in the case of anticancer therapy involving MAbs, or
- within 2 weeks prior to the first dose of KTN3379 in the case of palliative radiation therapy.
- Symptomatic or untreated central nervous system metastases requiring concurrent treatment, including but not limited to surgery, radiation, and/or corticosteroids; if treated, subject must be asymptomatic for 3 months prior to study entry
- Subjects who are known to have a history of or active human immunodeficiency virus (HIV) or active hepatitis B and/or C
- Uncontrolled intercurrent illness including but not limited to ongoing or active infection, symptomatic congestive heart failure, uncontrolled hypertension, uncontrolled or idiopathic hypotension, unstable angina pectoris, cardiac arrhythmia including atrial fibrillation, active peptic ulcer disease or gastritis, or psychiatric illness/social situations that would limit compliance with study requirements or compromise the ability of the subject to give written informed consent
- Any condition that, in the opinion of the investigator, would interfere with evaluation of the investigational product or interpretation of subject safety or study results
- Subjects with a left ventricular cardiac ejection fraction < 50% as assessed by an echocardiogram or MUGA scan

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02014909
United States, Colorado | |
Sarah Cannon Research Institute | |
Denver, Colorado, United States, 80218 | |
United States, Connecticut | |
Yale Cancer Center | |
New Haven, Connecticut, United States, 06511 | |
United States, Michigan | |
Barbara Ann Karmanos Cancer Institute | |
Detroit, Michigan, United States, 48201 | |
United States, Pennsylvania | |
University of Pennsylvania Perelman School of Medicine | |
Philadelphia, Pennsylvania, United States, 19104 | |
United States, Tennessee | |
Sarah Cannon Research Institute | |
Nashville, Tennessee, United States, 37203 |
Responsible Party: | Celldex Therapeutics |
ClinicalTrials.gov Identifier: | NCT02014909 |
Other Study ID Numbers: |
KTN3379-CL-001 |
First Posted: | December 18, 2013 Key Record Dates |
Last Update Posted: | July 24, 2017 |
Last Verified: | July 2017 |
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