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An Open Label, Multicenter, Phase I Extension Study of an Oral Cdk Inhibitor P1446A-05 Administered With an Oral BRAF Inhibitor Vemurafenib (Zelboraf®) in Patients With Advanced or Inoperable Malignant Melanoma With BRAF Mutation


Phase 1/Phase 2
18 Years
N/A
Not Enrolling
Both
Advanced or Inoperable Malignant Melanoma With BRAF Mutation

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Trial Information

An Open Label, Multicenter, Phase I Extension Study of an Oral Cdk Inhibitor P1446A-05 Administered With an Oral BRAF Inhibitor Vemurafenib (Zelboraf®) in Patients With Advanced or Inoperable Malignant Melanoma With BRAF Mutation


Inclusion Criteria:



1. Patients having histologically confirmed unresectable (Stage III) or metastatic
(Stage IV) malignant melanoma with a positive BRAF mutation result determined by
Roche CoDx or local CLIA-certified analysis

2. Patients naïve to a selective BRAF inhibitor therapy or must have progressed after
therapy on a selective BRAF inhibitor. For patients entering the protocol progressing
on vemurafenib therapy, they must be tolerant of the 960 mg po bid dose.

3. Tumor biopsies are optional in this study except for patients entering the mandatory
biopsy cohorts. Nevertheless tumor biopsies are encouraged, especially in patients
with accessible tumors for biopsy to include the collection of formalin-fixed,
paraffin-embedded (FFPE) and fresh- frozen tissue (FF) as outlined in the biomarker
sections of the protocol. Willingness of patient to give consent of biopsy, should be
ascertained

4. Patients of ≥ 18 years of age

5. Patients with Eastern Cooperative Oncology Group (ECOG) performance status 0 or1

6. Patients with measurable disease per 'Response Evaluation Criteria In Solid Tumors'
(RECIST version 1.1)

7. Patients must have normal organ and adequate marrow function

8. Patients with ability to swallow and retain oral medication

9. Women of childbearing potential and men willing to agree to use adequate
contraception (hormonal or barrier method of birth control; abstinence) prior to
study entry, during the duration of study participation and for at least 4 weeks
after withdrawal from the study, unless they are surgically sterilized.

10. Negative serum pregnancy test within 10 days prior to commencement of therapy dosing
in premenopausal women. Women of non-childbearing potential may be included if they
are either surgically sterile or have been postmenopausal for ≥1 year.

11. Ability to understand and the willingness to offer a written Informed Consent
document prior to the screening procedures for participation into the study

- For Extension phase-

- For patients entering the protocol progressing on vemurafenib therapy, they must
be tolerant of the vemurafenib dose selected for the extension phase

Exclusion Criteria:

1. Prior malignancy (within the last 2 years) except for adequately treated basal cell
or squamous cell skin cancer, in situ cervical cancer, in situ breast cancer, in situ
prostate cancer or any other cancer for which the patient has been disease-free for
at least 2 years

2. Patients who have received any prior chemotherapy, radiotherapy, biologic/targeted
anti-cancer therapy (one week for BRAF inhibitor for melanoma) or surgery within 4
weeks (6 weeks for monoclonal antibodies, radioactive monoclonal antibodies or any
radio-or toxin-immunoconjugates) before Day 1 of Investigational product
administration and have not recovered (to < Grade 1) from the toxic effects from any
prior therapy

3. Patients having received any other investigational agents within 4 weeks prior to Day
1 of Investigational product administration and have not recovered completely (to <
Grade 1) from the side effects of the earlier investigational agent

4. Anticipated administration of any anti-cancer therapies (chemotherapy, radiation
therapy, immunotherapy, biological therapy, hormonal therapy, surgery, and/or tumor
embolisation) other than those administered in this study such as BRAF inhibitor

5. Patients with symptomatic or untreated leptomeningeal or brain metastases, or spinal
cord compression [patients with previous brain metastases will be allowed to enter
the trial if metastases have been surgically removed or all known sites of metastases
have been treated with stereotactic high dose radiosurgery. Patients must be off
corticosteroids for at least one month and have a stable lesion with verification by
imaging (CT/MRI) within 28 days prior to Day 1 of Investigational product
administration]

6. Patients with clinically significant medical condition of malabsorption, inflammatory
bowel disease, chronic diarrheal condition, refractory nausea, vomiting or any other
condition that will interfere significantly with the absorption of study drugs

7. Patients with mean QTc interval >480 msec at screening

8. Treatment with drugs with potential to cause dysrhythmias including but not limited
to terfenadine, quinidine, procainamide, diisopyramide, sotalol, probucol, bepridil,
haloperidol, risperidone and/or indapamide

9. Patients on warfarin treatment

10. Any condition for which participation in this study as judged by the Investigator to
be detrimental to the patient with (such as) inter-current illness including, but
not limited to ongoing or active infection, New York Heart Association functional
classification class III, or IV heart failure; unstable angina pectoris; cardiac
arrhythmia; history of myocardial infarction; uncontrolled hypertension (blood
pressure above 160/100 mm Hg despite antihypertensive treatment); coronary artery
bypass graft; cerebrovascular accident; transient ischemic attack or pulmonary
embolism during the previous 6 months or psychiatric illness/social situations that
would jeopardize compliance with study requirements

11. Patients with a known immediate or delayed hypersensitivity reaction or idiosyncrasy
to any other medication chemically related to P1446A-05 or vemurafenib, or excipients
considered to be clinically significant by the investigator

12. Nursing woman

13. Patients with known HIV positivity or AIDS- related illness, or active Hepatitis B
virus, and active Hepatitis C virus

14. Patients taking drugs known to prolong the QTc interval who cannot be switched to an
alternative drug.

For Extension phase-

1. Patients with active second malignancy will be eligible as long as they do not need
systemic therapy for the second malignancy

2. Patients with active brain metastases will be included in the study as long as the
tumor size is less than 1 cm without the requirement of steroid use for neurological
symptoms

3. Patients with evaluable metastatic disease will be allowed even if there is no
measurable disease per RECIST 1.1. In this case patients with many sub centimeter
in-transit skin/SQ nodules will be eligible for the biopsy cohort.

Type of Study:

Interventional

Study Design:

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Maximum Tolerated Dose and Dose Limiting Toxicity

Outcome Description:

The study will be conducted in two phases- Phase I (Dose escalation phase), and Extension phase. In the Dose escalation' phase patients will be co-administered P1446A-05 (150, 250, 350 mg qd) and vemurafenib (720, 960 mg bid) in a cohort of three to six patients on a 28-day cycle, until the occurrence of disease progression or unacceptable toxicity. Escalation to the next higher dose during the dose escalation phase will depend upon demonstrated safety in the previous dose group. The maximum tolerated dose (MTD) of P1446A-05 and vemurafenib co-administered will be determined. In the 'Extension' phase, sixty patients with BRAF V600E/K mutations (forty patients naïve to selective BRAF inhibitor therapy, and twenty progressing on selective BRAF inhibitor therapy) will be treated at the MTD on a 28-day cycle, until the occurrence of disease progression or unacceptable toxicity to determine efficacy of the co-administration.

Outcome Time Frame:

Until disease progression or unacceptable toxicity (expected to be 6-8 months)

Safety Issue:

Yes

Principal Investigator

Adil Daud, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

UCSF Medical Center at Mount Zion

Authority:

United States: Food and Drug Administration

Study ID:

P1446A-05/72/12

NCT ID:

NCT01841463

Start Date:

May 2013

Completion Date:

March 2016

Related Keywords:

  • Advanced or Inoperable Malignant Melanoma With BRAF Mutation
  • Malignant Melanoma
  • Melanoma

Name

Location

The University of Texas, MD Anderson Cancer CenterHouston, Texas  77030
UCSF Medical Center at Mount ZionSouth San Francisco, California  94115