A Study of KX2-391 With Paclitaxel in Patients With Solid Tumors

Breast Cancer Clinical Trial

Official title:

An Open-label Phase I/II Study of KX2-391 in Combination With Paclitaxel in Patients With Advanced Solid Tumors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01764087
• Other study ID #: HM-KXI-101
• Status: Recruiting
• Phase: Phase 1/Phase 2
• First received: January 2, 2013
• Last updated: May 15, 2015
• Start date: December 2012
• Est. completion date: May 2016

Study information

• Verified date: March 2014
• Source: Hanmi Pharmaceutical Company Limited
• Contact: Seock-Ah Im, M.D., Ph.D.
• Phone: +82-2-2072-0850
• Is FDA regulated: No
• Health authority: Korea: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is to determine the maximum tolerated dose (MTD) of KX2-391 in Combination with paclitaxel in Phase I, and to evaluate the efficacy of KX2-391 in combination with paclitaxel in patients who are diagnosed as gastric and breast cancer, respectively in Phase II.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: May 2016
• Est. primary completion date: December 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years and older

Eligibility

Inclusion Criteria:

Phase I Portion:

• Diagnosis of solid tumors on histopathological examination or cytological examination for which no standard of care is available or conventional treatment modalities have no therapeutic effect at the time of entering into the study

Phase II Portion:

• Diagnosis of advanced/metastatic/recurrent stomach cancer or breast cancer on histopathological examination or cytological examination for which no standard of care is available or conventional treatment modalities have no therapeutic effect at the time of entering into the study

• Subjects with stomach cancer without prior taxane therapy

• Subjects with breast cancer with prior taxane therapy

• (Optional) Providing exploratory biomarker informed consent form to obtain archival tumor tissue and/or new tumor biopsy sample

Common:

1. Based on clinical screening,

? If radiotherapy was given, at least 4 weeks should have passed from the last treatment date and the patient should have recovered from the toxicity (However, for limited regional radiotherapy, at least 2 weeks from the last treatment date)

? If hormonal therapy was given, at least 2 weeks should have passed from the last treatment date and the patient should have recovered from the toxicity.

? If chemotherapy was given, at least 3 weeks should have passed from the last treatment date and the patient should have recovered from the toxicity (However, for nitrosourea or mitomycin, at least 6 weeks)

2. Aged = 20 years

3. ECOG (Eastern Cooperative Oncology Group) = 2

4. Life expectancy = 12 weeks

5. Should meet the followings,

? Bone marrow function ANC (Absolute Neutrophil Count) = 1.5 X 109/L, PLT (Platelet Count) = 100 X 109/L, Hemoglobin = 9.0 g/dl (In the case of hemoglobin of < 9.0 g/dl, the patient can be enrolled if the value is reversed to = 9.0 g/dl.)

? Kidney function Creatinine Clearance > 50 ml/min or Serum Clearance = 1.5 mg/dl

? Liver function AST (Aspartate Aminotransferase)/ALT (Alanine Aminotransferase)/ALP (Alkaline Phosphatase) = 3.0 X UNL and Total bilirubin = 2.0 mg/dl (With bone metastasis, ALP = 5.0 X UNL)

6. At least one measurable lesions with the length of the longest diameter of = 10 mm on spiral CT or multidetector CT or = 20 mm on conventional CT

7. Subjects who voluntarily consent to participate in this study and sign the written informed consent form

Exclusion Criteria:

1. Uncontrolled central nervous system metastasis

2. Malignant ascites requiring surgical treatment

3. Subjects who have blood malignancies including leukemia; or who have received or will receive bone marrow transplantation

4. Severe concurrent diseases as follows,

? History of unstable angina, heart failure, atrial or ventricular arrhythmia requiring pharmacological treatment, or having received treatment for myocardial infarction within 6 months (however, may be included under the judgment of the investigator if medically controlled), heart failure of Class III or IV by New York Heart Association Classes, or left ventricular ejection fraction of < 40%

? Receiving therapeutic dose administration of coumarin-type anticoagulants (however, up to 2 mg daily is permitted for line opening)

? Uncontrolled diabetes (fasting plasma glucose > 2.0 X UNL), severe hypertension, thyroid disorder and active infectious disease

? Psychiatric or neurological history including dementia or epilepsy which may threaten the compliance with this protocol

? A condition not allowing oral application of tablet formulation, and any clinically significant gastrointestinal abnormalities which may interfere with taking, passing or absorption of the study drug

5. Using disallowed concomitant medications (strong CYP3A4 (Cytochrome P450 3A4) inhibitors or inducers) (When a patient is using any of the disallowed concomitant medications below, wash-out of 1 week from the medication date is required)

6. Received other investigational product within 4 weeks prior to the administration of this study drug

7. Pregnant or breast-feeding women (however, women with 12 months of natural (spontaneous) amenorrhea or surgical bilateral oophorectomy (alone or with hysterectomy) at least 6 weeks ago, with appropriate clinical profile (e.g., appropriate age, history of vasomotor symptoms), will be considered women postmenopausal and of non-childbearing potential. In the case of oophorectomy alone, a woman will be considered to be of non-childbearing potential only if her reproductive condition is confirmed by follow-up hormone level assessment)

8. History of hypersensitivity to paclitaxel, compounds with similar chemical structure, or cremophor (polyoxyethylated castor oil) ingredient

9. Neuropathy of grade = 3 based on clinical screening

10. Known history of hepatitis B or C and known history of HIV serum positive

11. Others unable to participate in the study under the judgment of the investigator

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer
• Gastric Cancer
• Unspecified Adult Solid Tumor, Protocol Specific

Intervention

Drug:
• KX2-391 and Paclitaxel
A treatment cycle in phase I will consist of 28 days, according to the following schedule: KX2-391 20 mg PO once daily, Weekly paclitaxel 80 mg/m2 given intravenously over 1 hour on day 1, 8, and 15 of a 28 day cycle. The trial will initially test the combination of weekly paclitaxel and KX2-391 given PO, once daily , continuously. In case of 2 dose-limiting toxicities (DLT) in the first cohort, this intervention will be terminated A treatment cycle in phase II will consist of 28 days, according to the following schedule: KX2-391 MTD PO once daily, Weekly paclitaxel 80 mg/m2 given intravenously over 1 hour on day 1, 8, and 15 of a 28 day cycle.

Locations

Country	Name	City	State
Korea, Republic of	Seoul National University Bundang Hospital	Seongnam	Gyeonggi-Do
Korea, Republic of	Seoul National University Hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Hanmi Pharmaceutical Company Limited

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Pharmacodynamic (PD) Evaluation in Phase I Portion	Pre-dose and post-dose tubulin inhibition in peripheral blood monocytes extracted from blood samples, as measured by immunofluorescence staining	Time points at day 0 and 1 in cycle 1	No
Other	Exploratory Biomarker Evaluation in Phase II Portion	Pre-dose and post-dose Src signaling inhibition (p-Src and Ki-67) in archival tumor tissue and new biopsy sample, as measured by immunohistochemistry	Time points at day -6 and day 0	No
Primary	Dose-limiting Toxicities (DLTs) in Phase I Portion	Maximum tolerated dose (MTD) of KX2-391 in combination with weekly paclitaxel as determined by number of participants With DLTs related to KX2-391 in combination with weekly paclitaxel	From start of the treatment to end of cycle 1, which are 4 weeks	Yes
Primary	Tumor Overall Response Rates (ORRs) in Phase II Portion	The efficacy (overall response rate; ORR; complete response (CR) + partial response (PR)) of KX2-391 in combination with weekly paclitaxel at the MTD established during the phase I portion of this trial based on Response Evaluation Criteria in Solid Tumor (RECIST) 1.1	In every 2 cycles up to end of the treatment, an expected average of 16 weeks	No
Secondary	Pharmacokinetic (PK) Evaluation in Phase I Portion	PK parameters, including but not limited to, plasma concentration, AUC (Area Under Curve) 0-t, Cmax, Tmax, and T1/2 of KX2-391 alone and in combination with weekly paclitaxel	Time points at day 0, 1 and 8 in cycle 1	No
Secondary	The Preliminary Efficacy Data in Phase I Portion	The preliminary efficacy of KX2-391 in combination with weekly paclitaxel as determined by ORRs based on RECIST 1.1	In every 2 cycles up to end of the treatment, an expected average of 8 weeks	No
Secondary	Safety in Phase II Portion	Adverse events and their frequency, duration and severity, physical examination, laboratory parameters, vital signs and ECG change monitoring as determined based on CTCAE (Common Toxicity Criteria for Adverse Effects) 4.03	From start of the treatment to end of the treatment, an expected average of 16 weeks	Yes
Secondary	The Efficacy Data in Phase II Portion	Overall survival (OS), progression free survival (PFS), time to tumor progression (TTP) and duration of response	Up to die, an expected average of 24 weeks	No
Secondary	Pharmacokinetic (PK) Evaluation in Phase II Portion	PK parameters, including but not limited to, plasma concentration, AUC0-t, Cmax, Tmax, and T1/2 of KX2-391 alone and in combination with weekly paclitaxel	Time points at day 1 and 8 in cycle 1	No