Phase I Dose Escalation Study With an Allosteric AKT 1/2 Inhibitor in Patients

NCT ID: NCT01915576

Last Updated: 2016-12-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 79 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-09-30
• Study Completion Date: 2016-12-31

Brief Summary

This is the first study where BAY1125976 is given to humans. Patients (all comers) will receive the study drug treatment in a dose-escalation scheme (no placebo group) to determine the safety, tolerability and maximum tolerated dose (MTD) of BAY1125976. The relative bioavailability of liquid service formulation and tablets will be determined.

After the MTD is defined breast cancer patients with and without AKT1 mutation will be treated.

The study will also assess the pharmacokinetics, biomarker status, pharmacodynamic parameters and tumor response of BAY1125976.

BAY1125976 will be given daily as single oral application. Treatment will be stopped if the tumor continues to grow, if side effects, which the patient cannot tolerate, occur or if the patient decides to exit treatment.

Conditions

Neoplasms

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

BAY1125976 [once daily, dose-esc.]

Oral administration once daily. Starting dose is 10 mg and will be escalated depending on any dose-limiting toxicities

Group Type: EXPERIMENTAL

BAY1125976

Intervention Type: DRUG

Oral administration once daily. Starting dose is 10 mg and will be escalated depending on any dose-limiting toxicities

BAY1125976 [twice daily, dose-esc.]

Oral administration twice daily. Starting dose is 40mg twice daily and will be escalated depending on any dose-limiting toxicities

Group Type: EXPERIMENTAL

BAY1125976

Intervention Type: DRUG

Oral administration twice daily. Starting dose is 40mg twice daily and will be escalated depending on any dose-limiting toxicities

BAY1125976 [MTD]

Oral administration of the defined MTD which shows optimal safety, PK profile, PD target inhibition and preliminary efficacy (once daily or twice daily) in different patient groups

Group Type: EXPERIMENTAL

BAY1125976

Intervention Type: DRUG

Oral administration of the defined MTD which shows optimal safety, PK profile, PD target inhibition and preliminary efficacy (once daily or twice daily) in different patient groups

Interventions

BAY1125976

Oral administration once daily. Starting dose is 10 mg and will be escalated depending on any dose-limiting toxicities

Intervention Type: DRUG

BAY1125976

Oral administration twice daily. Starting dose is 40mg twice daily and will be escalated depending on any dose-limiting toxicities

Intervention Type: DRUG

BAY1125976

Oral administration of the defined MTD which shows optimal safety, PK profile, PD target inhibition and preliminary efficacy (once daily or twice daily) in different patient groups

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• For dose escalation cohorts: Subjects with advanced, histologically or cytologically confirmed solid tumors are eligible. Subjects' tumors (all comers) must be refractory to standard treatment with no standard therapy available, or subjects actively refuse any treatment, which would be regarded standard. In addition, the investigator must judge the experimental treatment as clinically and ethically acceptable
• For expansion cohort only: Subjects with histologically or cytologically proven metastatic breast cancer (with and without AKT1 E17K (G49A) mutation) or subjects with known AKT1 E17K (G49A) mutation in any other advanced solid tumor with at least one line of chemotherapy in the metastatic setting and not amenable to surgery with curative intent
• Subjects must have measurable disease (Response evaluation criteria in solid tumors (RECIST 1.1)
• Eastern Cooperative Oncology Group (ECOG) Performance Status 0 - 2
• Bone marrow, liver and renal functions as assessed by adequate laboratory methods to be conducted within 7 days prior to starting study treatment
• Subjects must provide tumor biopsies before treatment
• Recovery to CTCAE (Common Terminology Criteria for Adverse Events Version 4.03) Grade 0 or Grade 1 or recovery to baseline preceding the prior treatment of any previous drug / procedure-related toxicity (except alopecia, anemia, and hypothyroidism)

Exclusion Criteria

• History of cardiac disease including congestive heart failure > New York Heart Association (NYHA) Class II
• Subjects with type 1 or type 2 diabetes mellitus
• Subjects with fasting glucose >125 mg/dL in 2 independent measurements or glycated hemoglobin (HbA1c) ≥ 7%
• Moderate and severe hepatic impairment, i.e. Child-Pugh B or C
• Active infections of CTCAE (Common Terminology Criteria for Adverse Events Version 4.03) Grade >2 or infections of CTCAE Grade 2 not responding to therapy
• Symptomatic metastatic brain or meningeal tumors unless the patient is > 3 months from definitive therapy, has a negative imaging study within 4 weeks of study entry and is clinically stable with respect to the tumor at the time of study entry.
• Subjects undergoing renal dialysis
• Previous or concurrent cancer that is distinct in primary site or histology from the cancer being evaluated in this study except cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors (Ta, Tis & T1) or any cancer curatively treated > 3 years prior to study entry
• Autologous bone marrow transplant or stem cell rescue within 4 months of study entry
• Treatment with oral steroids (dose ≥ 10 mg/day of methylprednisolone or equivalent)
• Clinically relevant findings in the ECG such as a second- or third-degree AV block, prolongation of the QRS complex over 120 msec or of the QTcF-interval over 450 msec
• Acute toxic effects of previous anticancer chemotherapy or immunotherapy have to be normalized to CTCAE Grade equal or lower than 1 (excluding alopecia)

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Bayer

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bayer Study Director

Role: STUDY_DIRECTOR

Bayer

Locations

Santa Monica, California, United States

Boston, Massachusetts, United States

St Louis, Missouri, United States

Houston, Texas, United States

Villejuif, , France

Heidelberg, Baden-Wurttemberg, Germany

Sankt Gallen, Canton of St. Gallen, Switzerland

Countries

United States; France; Germany; Switzerland

Other Identifiers

2012-004671-39

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

16447

Identifier Type: -

Identifier Source: org_study_id