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BAY 1000394 for MCL-1-, MYC-, and CCNE1-Amplified Tumors

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ClinicalTrials.gov Identifier: NCT02656849
Recruitment Status : Withdrawn (Development of BAY1000394 has been terminated by Bayer.)
First Posted : January 15, 2016
Last Update Posted : July 1, 2016
Information provided by (Responsible Party):
Geoffrey Shapiro, MD, PhD, Dana-Farber Cancer Institute

Brief Summary:
This research study is studying whether a new experimental cancer study drug BAY 1000394 will be helpful in treating solid tumor cancer with an abnormality in one of the following genes: Mcl-1, Myc or CCNE.

Condition or disease Intervention/treatment Phase
Solid Tumor Drug: BAY 1000394 Phase 2

Detailed Description:
  • This research study is a Phase II clinical trial. Phase II clinical trials test the effectiveness of an investigational drug to learn whether the drug works in treating a specific cancer.
  • "Investigational" means that the drug is still being studied and that research doctors are trying to find out more about it-such as the safest dose to use, the side effects it may cause, and if the drug is effective for treating different types of cancer.
  • It also means that the FDA (the U.S. Food and Drug Administration) has not approved BAY 1000394 for use in participants with your type of cancer.
  • The study drug is a pan-CDK inhibitor targeting the genetic defect in several tumors, MCL1, Myc, or CCNE.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase II Study of BAY 1000394 in MCL1-Amplified, MYC-Amplified, CCNE1-Amplified Tumors
Study Start Date : February 2016
Estimated Primary Completion Date : October 2019
Estimated Study Completion Date : May 2023

Arm Intervention/treatment
Experimental: BAY 1000394

After the screening procedures confirm eligibility to participate in the research study:

  • Each treatment cycle lasts 4 weeks.
  • Participants will take the study drug orally at predetermined times and dosage per cycle.
Drug: BAY 1000394
Other Name: Roniciclib

Primary Outcome Measures :
  1. Six-month progression-free survival rate [ Time Frame: six months ]
    RECIST 1.1

Secondary Outcome Measures :
  1. Response Rate Mcl1-amplified tumors [ Time Frame: six months ]
    RECIST 1.1

  2. Response Rate MYC-amplified tumors [ Time Frame: six months ]
    RECIST 1.1

  3. Response Rate CCNE1-amplified tumors [ Time Frame: six months ]
    RECIST 1.1

  4. Overall Survival [ Time Frame: six months ]
    Kaplan Meier analysis

  5. Time to Progression [ Time Frame: six months ]
    RECIST 1.1

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patients must have advanced cancer for which no curative therapy exists and have a malignancy which matches one of the following cohorts:

    • MCL1 amplification (≥ 3 fold);
    • MYC amplification (≥ 6 fold);
    • CCNE1 amplification (≥ 6 fold).
    • Molecular abnormalities may be detected by any CLIA-certified test, including Massive Parallel (Next-Generation) sequencing platforms.
  • Patients must have measurable disease as defined by RECIST 1.1 criteria. In selected cases patients with evaluable disease may be eligible after discussion between the PI and Bayer.
  • Participants must have completed at least one line of therapy in the advanced/metastatic setting prior to enrollment
  • Participants with advanced disease for which approved second-line options exist will be eligible when they have progressed beyond such approved second-line therapy
  • Age ≥ 18 years. Because there is no data for evaluating these compounds in pediatric populations, the appropriate clinical trial can be conducted in the future in this specific population.
  • ECOG performance status of 0-1 (Karnofsky ≥70%, see Appendix A)
  • Life expectancy of greater than 12 weeks
  • Adequate bone marrow, liver, and renal functions as assessed by the following laboratory requirements:

    • Hemoglobin ≥8.5 g/dL
    • Absolute neutrophil count (ANC) ≥2 x 10/9/L
    • Platelet count ≥100 x 10/9/L
    • Total bilirubin ≤1.5 times the upper limit of normal (ULN)
    • Alanine aminotransferase (ALT) and aspartate transaminase (AST) ≤2.5 x ULN (≤5 x ULN for subjects with liver involvement of their cancer)
    • Prothrombin time-international normalized ratio (PT-INR) and partial thromboplastin time (aPTT) ≤1.5 x ULN
    • Estimated glomerular filtration rate (eGFR) ≥60 mL/min per 1.73 m/2 according to the Cockcroft-Gault formula
  • Negative serum pregnancy test in women of childbearing potential (WOCBP)(performed within 7 days of randomization). Negative results must be available prior to study treatment administration
  • Women of childbearing potential and men must agree to use adequate barrier birth control measures from the time of signing of the informed consent form until at least 3 months after the last study drug administration. The investigator or a designated associate is requested to advise the subject on how to achieve adequate birth control. Adequate contraception is defined in the study as any medically recommended method (or combination of methods) as per standard of care. These procedures should be documented in source documents. Postmenopausal women are defined as:

    • Age >50 years with amenorrhea for at least 12 months or
    • Age ≤50 years with 6 months of spontaneous amenorrhea and follicle stimulating hormone level within postmenopausal range (>40 mIU/mL) or
    • Bilateral oophorectomy
    • Additional adequate contraception which includes hormonal contraception with implants or combined oral contraceptives, certain intrauterine devices, bilateral tubal ligation, hysterectomy, or vasectomy of the partner is allowed as long as a barrier method is also being used
    • Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria:

  • Prior radiotherapy is permitted but must have occurred ≥2 weeks (palliative radiotherapy) or ≥ 4 weeks (curative radiotherapy) and subject must have no Grade 3 or 4 toxicities prior to first dose of study treatment
  • Prior chemotherapy is allowed. Patients must not have received chemotherapy for 3 weeks prior to the initiation of study treatment and must have full recovery from any acute effects of any prior chemotherapy. Patients must not have had nitrosoureas or mitomycin C for 6 weeks prior to the initiation of study treatment.
  • Prior exposure to approved receptor tyrosine kinase inhibitors is permitted. At least 5 half-lives must have elapsed since the completion of the kinase inhibitor and the initiation of study treatment.
  • Prior experimental (non-FDA approved) therapies and immunotherapies are allowed. Patients must not have received these therapies for 4 weeks prior to the initiation of study treatment and must have full recovery from any acute effects of these therapies.
  • Participants must not have received pan-cyclin-dependent kinase inhibitors as prior therapy.
  • Current or ongoing administration of anticoagulation or antiplatelet therapy. However, use of low-dose aspirin (≤100 mg/day) and/or low-dose heparin is permitted unless it is being used for conditions other than cancer
  • Known hypersensitivity to any of the study treatments or excipients of the preparations or any agent given in association with this study
  • Previous deep vein thrombosis (within the last 6 months), arterial thrombotic events (including strokes), or pulmonary embolism
  • History of cardiac disease: Congestive heart failure New York Heart Association (NYHA) Class III or IV angina (within past 6 months prior to study entry), myocardial infarction, or cardiac arrhythmias requiring anti-arrhythmic therapy (beta blockers or digoxin are permitted)
  • Known human immunodeficiency virus infection, active hepatitis B or C, or chronic hepatitis B or C requiring treatment with antiviral therapy
  • Active clinically serious infections of NCI-CTCAE v4.0 >Grade 2
  • Seizure disorder requiring therapy (such as steroids or anti-epileptics)
  • Concomitant use of other medications that are known to lower the seizure threshold
  • Symptomatic metastatic brain or meningeal tumors, including those of the spinal cord, and including cases of neoplastic meningitis (also known as carcinomatous meningitis or leptomeningeal carcinomatosis).
  • History of organ allograft
  • Evidence or history of bleeding disorder, i.e. any hemorrhage / bleeding event of NCI-CTCAE v4.0 >Grade 2 within 4 weeks prior to the first dose of study treatment
  • Uncontrolled hypertension (systolic blood pressure >150 mmHg or diastolic blood pressure >90 mmHg despite optimal medical management)
  • Serious, non-healing wound, ulcer, or bone fracture (bone fractures due to bone metastases are acceptable)
  • Subjects on dialysis
  • Sensory neuropathy with sensory alterations or paresthesia (including tingling), interfering with function (≥NCI-CTCAE v4.0 Grade 2)
  • Previous or coexisting cancer that is distinct from the study indication and has not been curatively treated >3 years prior to study entry EXCEPT cervical cancer in-situ, treated basal cell carcinoma, superficial bladder tumors (Ta and Tis)
  • Any condition that is unstable or could jeopardize the safety of the subject and his/her compliance in the study
  • Subjects unable to swallow oral medications
  • Any malabsorption condition
  • Major surgery, open biopsy, or significant trauma within 4 weeks prior to the first dose of study treatment is excluded (central line surgery is not considered major surgery)
  • Autologous bone marrow transplant or stem cell rescue within 4 months prior to first dose of study treatment is not allowed
  • Investigational drug treatment outside of this study during or within 4 weeks prior to study entry. Toxic effects of previous investigational drug treatment have to be normalized
  • Potent CYP3A4 inhibitors and CYP3A inducers (see Appendix B)
  • Pregnant or breast-feeding women

Information from the National Library of Medicine

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): NCT02656849

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United States, Massachusetts
Dana Farber Cancer Institute
Boston, Massachusetts, United States, 02115
Sponsors and Collaborators
Dana-Farber Cancer Institute
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Principal Investigator: Geoffrey Shapiro, MD, PhD Dana-Farber Cancer Institute
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Responsible Party: Geoffrey Shapiro, MD, PhD, Principal Investigator, Dana-Farber Cancer Institute
ClinicalTrials.gov Identifier: NCT02656849    
Other Study ID Numbers: 15-380
First Posted: January 15, 2016    Key Record Dates
Last Update Posted: July 1, 2016
Last Verified: June 2016
Keywords provided by Geoffrey Shapiro, MD, PhD, Dana-Farber Cancer Institute:
Solid Tumor
Additional relevant MeSH terms:
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