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Study of Anti-HB-EGF Antibody KHK2866 in Subjects With Advanced Solid Tumors and Ovarian Cancer

Phase 1
Terminated
Conditions
Neoplasms
Fallopian Tube Neoplasms
Primary Peritoneal Neoplasm
Ovarian Neoplasms
Interventions
Registration Number
NCT01279291
Lead Sponsor
Kyowa Kirin Co., Ltd.
Brief Summary

This is a two-part, Phase 1, open-label, multicenter, dose escalation study of KHK2866 as monotherapy in patients with advanced solid tumors, and in combination with chemotherapy in subjects platinum-sensitive and platinum-resistant ovarian cancer.

Detailed Description

During Phase 1a, groups of eligible patients with advanced solid tumors will receive KHK2866 as monotherapy in escalating doses. The Phase 1b portion will enroll patients with ovarian cancer who will receive KHK2866 in combination with one of three chemotherapy regimens (Arms): gemcitabine+carboplatin (platinum-sensitive, weekly paclitaxel (platinum-resistant), or pegylated liposomal doxorubicin (platinum-resistant). Escalating doses of the combination of KHK2866 and the chemotherapy regimen will given to two groups of subjects per Arm. The goal of the study is to learn about the side effects of KHK2866 alone or given in combination with chemotherapy. All subjects will receive study therapy for up to 6 cycles (up to 12 cycles for subjects assigned to PLD \[Arm 3 of Phase 1b\]), or until disease progression, the development of severe side effects, noncompliance or withdrawal of consent by the subject, or other removal criteria whichever comes first.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
22
Inclusion Criteria
  • Histologically or cytologically documented, measurable or non-measurable, advanced primary or recurrent solid tumor (Phase 1a only) which is unresponsive to standard therapy or for which there is no standard therapy available.
  • Histologically or cytologically documented ovarian, primary peritoneal, or fallopian tube cancer.
  • The subject has objective radiographic disease progression and either unmeasurable or measurable disease during or following the last treatment regimen, or serum cancer antigen-125 (CA-125) greater than 2X the upper limit of normal ([ULN] >70 U/mL
  • Life expectancy >3 months.
  • Performance status < 3 at study entry.
  • Age > 18 years.
  • Normal left ventricular ejection fraction.
  • Recovered from the effects of recent surgery, radiotherapy, chemotherapy, hormonal therapy, or other therapies for cancer
  • Preserved hepatic, renal, and hematopoetic organ function.
  • Male and female subjects must use medically accepted contraception.
Exclusion Criteria
  • Ovarian malignancy of low malignant potential.

  • Received anti-cancer chemotherapy, hormonal therapy, radiotherapy, immunotherapy, or investigational agents within 4 weeks prior to the first dose of KHK2866 (6 weeks for nitrosourea or mitomycin chemotherapy).

  • received Mabs or had major surgery within 4 weeks of the first dose of KHK2866.

  • Requires administration of a prohibited medication or treatment including: prophylactic use of erythroid and/or granulocyte colony stimulating factors; concurrent anti-cancer treatment; biologic response modifiers for any condition

  • Brain metastases, leptomeningeal or primary brain neoplasm, even if treated.

  • Previously untreated or uncontrolled epidural metastasis

  • Cerebrovascular accident, Transient ischemic attack; symptomatic head trauma, or seizures or any kind within 6 months

  • Dementia, or other disorders of mentation or difficulty speaking or difficulty with comprehension.

  • Suspected impending bowel obstruction

  • The subject is pregnant,or is lactating.

  • Significant uncontrolled intercurrent illness

  • Known HIV infection or AIDS-related illness.

  • Known active hepatitis B or C or other active liver disease.

  • Psychiatric illness, disability or social situation that would compromise the subject's safety, ability to provide consent, or limit his/her compliance with study requirements.

  • Experienced a unmanageable hypersensitivity reactions to Mabs or other therapeutic proteins.

  • History of second primary cancer, with the exception of: a) curatively resected non-melanomatous skin cancer; b) curatively treated cervical carcinoma in-situ; or c) other primary solid tumor treated with curative intent and no known active disease present and no treatment administered during the last 2 years.

  • Additional exclusion criteria for subjects proposed for enrollment into the Phase 1b portion:

    • History of hypersensitivity or infusion reaction to any of the proposed chemotherapy arm's agents that could not be controlled with pre-medication and/or infusion rate adjustment;
    • Prior treatment with KHK2866;
    • History of Grade ≥ 3 non-hematologic or Grade 4 hematologic toxicity attributable to any of the proposed chemotherapy arm's agents
    • For subjects proposed to receive treatment with KHK2866 plus PLD: prior total cumulative exposure to doxorubicin must be ≤ 240 mg/m2.
  • Subjects with a known history of interstitial lung disease or pulmonary fibrosis. Subjects must have pulse oximetry >88% on room air at rest, and a DLco of >49% if there is no evidence of lung metastasis.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
KHK2866 as monotherapyKHK2866Groups of subjects will receive a weekly infusions of KHK2866 as treatment for advanced cancer. If there no severe side effects, the dose will be increased for future subjects. A total of four groups are anticipated. Once an acceptable dose is determined an additional seven subjects will be treated at that dose.
KHK2866, gemcitabine+carboplatinKHK2866Open to subjects with ovarian, fallopian tube, or primary peritoneal cancer only. One group of subjects will receive one dose below the maximum tolerated dose of KHK2866 identified in Phase 1a along with gemcitabine and carboplatin. The dose of KHK2866 will be increased to the MTD for the next group if no severe side effects are noted. Once an acceptable dose is determined an additional seven subjects will be treated at that dose.
KHK2866, weekly paclitaxelKHK2866Open to subjects with ovarian, fallopian tube, or primary peritoneal cancer only. One group of subjects will receive one dose below the maximum tolerated dose of KHK2866 identified in Phase 1a along with weekly paclitaxel (80 mg/m2). The dose of KHK2866 will be increased to the MTD for the next group if no severe side effects are noted. Once an acceptable dose is determined an additional seven subjects will be treated at that dose.
KHK2866, pegylated liposomal doxorubicinKHK2866Open to subjects with ovarian, fallopian tube, or primary peritoneal cancer only. One group of subjects will receive one dose below the maximum tolerated dose of KHK2866 identified in Phase 1a along with monthly PLD (40 mg/m2). The dose of KHK2866 will be increased to the MTD for the next group if no severe side effects are noted. Once an acceptable dose is determined an additional seven subjects will be treated at that dose.
KHK2866, gemcitabine+carboplatinGemcitabine and CarboplatinOpen to subjects with ovarian, fallopian tube, or primary peritoneal cancer only. One group of subjects will receive one dose below the maximum tolerated dose of KHK2866 identified in Phase 1a along with gemcitabine and carboplatin. The dose of KHK2866 will be increased to the MTD for the next group if no severe side effects are noted. Once an acceptable dose is determined an additional seven subjects will be treated at that dose.
KHK2866, pegylated liposomal doxorubicinpegylated liposomal doxorubicinOpen to subjects with ovarian, fallopian tube, or primary peritoneal cancer only. One group of subjects will receive one dose below the maximum tolerated dose of KHK2866 identified in Phase 1a along with monthly PLD (40 mg/m2). The dose of KHK2866 will be increased to the MTD for the next group if no severe side effects are noted. Once an acceptable dose is determined an additional seven subjects will be treated at that dose.
KHK2866, weekly paclitaxelpaclitaxelOpen to subjects with ovarian, fallopian tube, or primary peritoneal cancer only. One group of subjects will receive one dose below the maximum tolerated dose of KHK2866 identified in Phase 1a along with weekly paclitaxel (80 mg/m2). The dose of KHK2866 will be increased to the MTD for the next group if no severe side effects are noted. Once an acceptable dose is determined an additional seven subjects will be treated at that dose.
Primary Outcome Measures
NameTimeMethod
Number of Participants with Adverse Events as a Measure of Safety and Tolerabilityat least 60 days, and up to 6 months

The safety of KHK2866 will be determined by reported adverse events (AEs), changes in physical examinations, vital sign measurements, electrocardiograms (ECGs), clinical laboratory evaluations, and treatment discontinuation due to toxicity.

Secondary Outcome Measures
NameTimeMethod
To evaluate the changes in serum HB-EGf in participants administered KHK2866at least 60 days, and up to 6 months

Participants will have serial blood samples taken to develop the PD profile.

To determine the Cmax, Tmax, AUC and half life of KHK2866 when administered i.v. as monotherapyat least 28 days and up to 6 months

Participants will have serial blood samples taken to determine the PK profile of the study drug.

To screen for the development of antibodies against KHK2866 (immunogenicity).at least 60 days and up to 6 months

Participants will have serial blood samples to check for the development of anti-KHK2866 antibodies.

To describe any anti-tumor activity observed when KHK2866 is administered i.v. as monotherapy, or in combination with chemotherapy.at least 60 days and up to 6 months

Trial Locations

Locations (7)

USC Norris Comprehensive Cancer Center

🇺🇸

Los Angeles, California, United States

Cedar Sinai-Samuel Oschin Comprehensive Cancer Institute

🇺🇸

Los Angeles, California, United States

Dana Farber Cancer Institute

🇺🇸

Boston, Massachusetts, United States

Massachusetts General Hospital

🇺🇸

Boston, Massachusetts, United States

Arizona Cancer Center

🇺🇸

Tucson, Arizona, United States

Cancer Therapy and Research Center

🇺🇸

San Antonio, Texas, United States

Oncology Consultants

🇺🇸

Houston, Texas, United States

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