Phase 1b/2 Study of U3-1287 in Combination With Trastuzumab Plus Paclitaxel in Newly Diagnosed Metastatic Breast Cancer (MBC)

Metastatic Breast Cancer Clinical Trial

Official title:

Randomized, Placebo Controlled, Double Blind Phase 1b/2 Study of U3-1287 (AMG 888) in Combination With Trastuzumab Plus Paclitaxel in Newly Diagnosed HER2 Positive Metastatic Breast Cancer (MBC)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01512199
• Other study ID #: U31287-A-U202
• Status: Terminated
• Phase: Phase 1/Phase 2
• First received: January 9, 2012
• Last updated: October 16, 2017
• Start date: November 2011
• Est. completion date: January 28, 2015

Study information

• Verified date: October 2017
• Source: Daiichi Sankyo, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase 1b/2 study. In Phase 1b portion, subjects will know the treatment they are receiving . Subjects will receive U3-1287 with trastuzumab plus paclitaxel . The phase 1b portion will determine if adding U3-1287 to trastuzumab plus paclitaxel will be safe in subjects with metastatic breast cancer. In phase 2 portion, subjects will be blinded to the treatments they are receiving . Subjects will receive either trastuzumab plus paclitaxel with U3-1287 or trastuzumab plus paclitaxel and placebo.The phase 2 portion will determine if adding U3-1287 to trastuzumab plus paclitaxel will be safe and improve survival in subjects with metastatic breast cancer.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 29
• Est. completion date: January 28, 2015
• Est. primary completion date: January 28, 2015
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

Subjects must satisfy all of the following criteria to be included in the study:

1. Women = 18 years old.

2. Histologically or cytologically confirmed adenocarcinoma of the breast with metastatic disease and at least 1 measurable lesion per Response Evaluation Criteria in Solid Tumors (RECIST) guidelines Version 1.1.

3. Documented HER2+ disease as measured by FISH or IHC (3+). See Appendix 17.8 for documentation criteria.

4. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.

5. Hematological function, as follows:

• Absolute neutrophil count (ANC) = 1.5 x 109/L

• Platelet count >100 x 109/L

• Hemoglobin =9 g/dL.

6. Renal function, as follows:

• Calculated creatinine clearance =60 mL/min using the modified Cockcroft Gault equation.

7. Hepatic function, as follows:

• AST =2.5 x ULN (if liver metastases are present, < 5 x ULN)

• ALT =2.5 x ULN (if liver metastases are present, < 5 x ULN)

• Alkaline phosphatase = 2.0 x ULN (if bone or liver metastases are present, < 5 x ULN)

• Bilirubin =1.5 x ULN.

8. Prothrombin time (PT) and partial thromboplastin time (PTT) =1.5 x ULN.

9. Availability of archived tumor sample or fresh tumor specimen (does not have to be provided by treatment start) to confirm HER2 status and for tumor biomarkers/mutation analysis.

10. Subjects must be postmenopausal (no menstrual period for a minimum of 12 months) or surgically sterile, or must use maximally effective birth control during the period of therapy, and be willing to use contraception for 6 months following the last investigational drug dose and have a negative urine or serum pregnancy test upon entry into this study if subject is of childbearing potential. Partners of subjects must be surgically sterile or willing to use a double barrier contraception method upon enrollment, during the course of the study, and for 6 months after last investigational drug dose received.

11. Subjects must be willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.

12. Subjects must be competent and able to comprehend, sign, and date an IEC- or IRB-approved ICF before performance of any study specific procedures or tests.

Exclusion Criteria:

Subjects who meet any of the following criteria will be disqualified from entering the study:

1. Prior treatment for metastatic disease other than radiation therapy. Neoadjuvant/adjuvant therapy with paclitaxel, and/or docetaxel, and/or trastuzumab is allowed if completed more than 12 months prior to relapse/progression.

2. Clinically active brain metastases, defined as untreated symptomatic, or requiring therapy with steroids or anticonvulsants to control associated symptoms. Subjects with treated brain metastases that are no longer symptomatic and require no treatment with steroids or anticonvulsants may be included in the study if they have recovered from the acute toxic effect of radiotherapy.

3. LVEF < 50%. History of LVEF decline to < 50% on prior trastuzumab therapy.

4. Therapeutic or palliative radiation therapy or major surgery within 4 weeks before study drug treatment.

5. History of other malignancies, except adequately treated nonmelanoma skin cancer, curatively treated in situ cancer, or other solid tumors curatively treated with no evidence of disease for = 5 years.

6. Uncontrolled hypertension (diastolic blood pressure > 100 mmHg or systolic blood pressure > 140 mmHg). Use of antihypertensive medications is permissible to maintain blood pressure within the required parameters.

7. Clinically significant electrocardiogram (ECG) changes that obscure the ability to assess the RR, PR, QT, QTc and QRS intervals.

8. Subjects with left bundle branch block, atrial fibrillation and use of a cardiac pacemaker specifically will be excluded.

9. Ascites or pleural effusion requiring chronic medical intervention.

10. Pre-existing peripheral neuropathy > grade 1.

11. Myocardial infarction, symptomatic CHF (New York Heart Association > Class II), unstable angina, or unstable cardiac arrhythmia requiring medication within 1 year before enrollment.

12. Use of cytochrome P450 (CYP) 3A4 (CYP3A4) or CYP2C8 inducers within 28 days prior to Day 1, use of CYP3A4 or CYP2C8 inhibitors within 14 days prior to Day 1, or concurrent use of CYP3A4 or CYP2C8 inducers or inhibitors (see Appendix 17.6 for list of CYP34A and CYP2C8 inhibitors and inducers).

13. Use of amiodarone within 6 months prior to enrollment.

14. Concurrent use of antiarrhythmic medications.

15. Participated in clinical drug studies within 4 weeks (2 weeks for small molecule tyrosine kinase inhibitors; 6 weeks for mitomycin C and nitrosoureas) before study drug treatment. Current participation in other investigational protocols or procedures.

16. Uncontrolled infection requiring IV antibiotics, antivirals, or antifungals.

17. Known human immunodeficiency virus (HIV) infection, or active hepatitis B or C infection.

18. History of hypersensitivity to any of the study drugs or to any excipients.

19. Serious intercurrent medical or psychiatric illnesses or any other conditions that in the opinion of the Investigator would impair the ability to give informed consent or unacceptably reduce protocol compliance or safety of the study treatment.

20. Pregnant, breastfeeding, or unwilling/unable to use acceptable contraception.

21. QTc interval > 450 msec by Friderica's formula on two successive screening measurements (second measurement is required if first measurement is > 450 msec.

22. Personal or family history of long-QT syndrome.

23. Subjects who are receiving drugs that may affect QTc (eg, quinidine or moxifloxacin).

Related Conditions & MeSH terms

• Breast Neoplasms
• Metastatic Breast Cancer

Intervention

Drug:
• U3-1287
U3-1287: 18 mg/kg administered intravenously once every three weeks
• Trastuzumab
Trastuzumab: 6 mg/kg up to 8 mg/kg administered intravenously once every three weeks
• Paclitaxel
Paclitaxel: 175 mg/m^2 administered intravenously once every three weeks
• U3-1287
The maximum tolerated dose as determined in Phase 1b portion (between 9 mg/kg and 18 mg/kg) administered intravenously once every three weeks
• Trastuzumab
Trastuzumab: 6 mg/kg up to 8 mg/kg administered intravenously once every three weeks
• Paclitaxel
Paclitaxel: 175 mg/m^2 administered intravenously once every three weeks
• Placebo
Placebo: Dose corresponding to U3-1287 administered intravenously once every three weeks

Locations

Country	Name	City	State
Argentina	Unidad de Investigación FP Clinical Pharma en Centro Medico Integral Fitz Roy	Acevedo	Ciudad Autónoma de Buenos Aires
Argentina	Hospital Britanico	Buenos Aires
Argentina	Sanatorio de la Providencia	Buenos Aires
Argentina	Instituto Damic - Fundacion Rusculleda	Cordoba
Argentina	Centro Medico San Roque	San Miguel	Tucuman
Argentina	ISIS Centro Especializado	Santa Fe
Chile	Instituto de Tereplas Oncologicas Providencia INTOP	Providencia	Santiago
Chile	Hospital Clinico San Borja Arriaran	Santiago

Sponsors (1)

Lead Sponsor	Collaborator
Daiichi Sankyo, Inc.

Countries where clinical trial is conducted

Argentina,  Chile, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Determination of the maximum tolerated dose based on the incidence of dose limiting toxicities (phase 1b only)	The following criteria will also be considered a dose limiting toxicity (DLT).; > 15% decrease in left ventricular ejection fraction (LVEF) from baseline or an LVEF value > 10% below lower limit of normal (LLN); Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 3 x the upper limit of normal (ULN) AND total bilirubin > 2 x ULN or international normalized ratio (INR) > 1.5	Study start to approximately 16 weeks
Primary	Progression Free Survival (Phase 2 only)	Tumor assessment will be conducted every 6 weeks independent of treatment cycle in accordance with Response Evaluation Criteria in Solid Tumors (RECIST version 1.1)	52 weeks (Start to end of Phase 2)
Secondary	Pharmacokinetics (Area Under Curve) of U3-1287 when combined with trastuzumab plus paclitaxel		Pharmacokinetic blood samples will be taken on days 1, 2, 3, 8, 15, end of study (phase 1b) and during cycles 1-5, 9, 13, and at the end of study (Phase 2)
Secondary	Pharmacokinetics (Area Under Curve Extrapolation Percent) of U3-1287 when combined with trastuzumab plus paclitaxel		Pharmacokinetic blood samples will be taken on days 1, 2, 3, 8, 15, end of study (phase 1b) and during cycles 1-5, 9, 13, and at the end of study (Phase 2)
Secondary	Pharmacokinetics (C-max, C-min) of U3-1287 when combined with trastuzumab plus paclitaxel		Pharmacokinetic blood samples will be taken on days 1, 2, 3, 8, 15, end of study (phase 1b) and during cycles 1-5, 9, 13, and at the end of study (Phase 2)
Secondary	Pharmacokinetics (T-max) of U3-1287 when combined with trastuzumab plus paclitaxel		Pharmacokinetic blood samples will be taken on days 1, 2, 3, 8, 15, end of study (phase 1b) and during cycles 1-5, 9, 13, and at the end of study (Phase 2)
Secondary	Pharmacokinetics (Terminal Elimination Rate Constant) of U3-1287 when combined with trastuzumab plus paclitaxel		Pharmacokinetic blood samples will be taken on days 1, 2, 3, 8, 15, end of study (phase 1b) and during cycles 1-5, 9, 13, and at the end of study (Phase 2)
Secondary	Pharmacokinetics (Terminal Half-Life) of U3-1287 when combined with trastuzumab plus paclitaxel		Pharmacokinetic blood samples will be taken on days 1, 2, 3, 8, 15, end of study (phase 1b) and during cycles 1-5, 9, 13, and at the end of study (Phase 2)
Secondary	Pharmacokinetics (Volume of Distribution) of U3-1287 when combined with trastuzumab plus paclitaxel		Pharmacokinetic blood samples will be taken on days 1, 2, 3, 8, 15, end of study (phase 1b) and during cycles 1-5, 9, 13, and at the end of study (Phase 2)
Secondary	Pharmacokinetics (Total Body Clearance) of U3-1287 when combined with trastuzumab plus paclitaxel		Pharmacokinetic blood samples will be taken on days 1, 2, 3, 8, 15, end of study (phase 1b) and during cycles 1-5, 9, 13, and at the end of study (Phase 2)
Secondary	The best overall tumor response rate (Phase 1b)	The best overall tumor response is defined as the best response among all overall responses (in the order of Complete Response, Partial Response, Stable Disease, and Progressive Disease as per RECIST Version 1.1) recorded from the start of treatment.	Study start to 16 weeks
Secondary	Human anti-human antibody (HAHA) profile for U3-1287 (Phase 1b only)	The presence of HAHA (anti-U3-1287 neutralizing antibody) in serum will be assessed. To determine the presence of HAHA, blood samples will be taken preinfusion on Day 1 and at end of study treatment visit.	Study start to 16 weeks
Secondary	Human anti-human antibody (HAHA) profile for U3-1287 (Phase 2)	The presence of HAHA (anti-U3-1287 neutralizing antibody) in serum will be assessed. To determine the presence of HAHA, blood samples will be taken preinfusion on Day 1 of Cycles 1, 2, 3, 5, 9, and 13, and at end of study treatment visit.	Study start to 52 weeks
Secondary	Overall survival (Phase 2)		Study start to 52 weeks
Secondary	Duration of response (Phase 2)		Study start to 52 weeks
Secondary	Time to response (Phase 2)		Study start to 52 weeks
Secondary	Time to progression (Phase 2)		Study start to 52 weeks
Secondary	Duration of stable disease (Phase 2)		Study start to 52 weeks
Secondary	The best overall tumor response rate (Phase 2)	The best overall tumor response is defined as the best response among all overall responses (in the order of Complete Response, Partial Response, Stable Disease, and Progressive Disease as per RECIST Version 1.1) recorded from the start of treatment.	Study start to 52 weeks
Secondary	Disease control rate (Phase 2)	The disease control rate is defined as the proportion of subjects with the best overall response of stable disease or better	Study start to 52 weeks