Dose-escalation Study of Oral CX-4945

Sponsor

Cylene Pharmaceuticals (Industry)

Overall Status

Unknown status

CT.gov ID

NCT00891280

Collaborator

(none)

Enrollment

Locations

33.9

Duration (Months)

13.8

Patients Per Site

0.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This Phase 1 study of oral CX-4945 is designed to test the safety, tolerability and highest safe dose level of this CK2 inhibitor in patients with advanced solid tumor cancers, Castleman's Disease or Multiple Myeloma.

Condition or Disease	Intervention/Treatment	Phase
Advanced Solid Tumors Breast Cancer Inflammatory Breast Cancer Castleman's Disease Multiple Myeloma	Drug: CX-4945 oral formulation	Phase 1

Detailed Description

Elevated CK2 activity has been associated with malignant transformation and aggressive tumor growth and overexpression of CK2 has been documented in multiple types of cancer. CK2 has emerged as a potential anticancer target and inhibition of CK2 represents a potential therapeutic strategy to target a specific molecular defect perpetuating many cancers. CX-4945 has demonstrated potent inhibition of CK2 enzymatic activity. This study will evaluate the safety, pharmacokinetics (PK), and pharmacodynamic (PD) effects of CX-4945 administered to patients with malignancies or lymphoproliferative disorders known to overexpress CK2 including advanced solid tumors, Multiple Myeloma and Castleman's Disease.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

55 participants

Allocation:

Non-Randomized

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase 1, Multi-Center, Open-Label, Dose-Escalation, Safety, Pharmacokinetic, and Pharmacodynamic Study of CX-4945 Administered Orally to Patients With Advanced Solid Tumors, Castleman's Disease or Multiple Myeloma

Study Start Date :

Feb 1, 2009

Anticipated Primary Completion Date :

Dec 1, 2011

Anticipated Study Completion Date :

Dec 1, 2011

Outcome Measures

Primary Outcome Measures

Safety (Dose limiting toxicities, maximum tolerated dose) [One year (Assessed at Cycle 1)]
Drug-related adverse events [One Year (Asessed from first administration of study drug through 30 days after the last dose)]

Secondary Outcome Measures

Pharmacokinetic and pharmacodynamic assessments [One Year (Assessed during Cycle 1)]
Observe evidence of antitumor activity [One Year (Assessed after every two cycles)]
Establish the recommended Phase 2 dose [One Year (Study completion)]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Histologically or cytologically confirmed malignancy or lymphoproliferative disorder known to over express CK2 which has failed standard therapies (surgery, radiotherapy, endocrine therapy, chemotherapy) or for which effective therapy is not available, including the following types: (examples)
Lung cancer
Renal cell cancer
Breast cancer
Inflammatory breast cancer
Head and neck cancer - squamous cell
Prostate cancer
Colorectal cancer
Castleman's disease (multi-centric disease)
Multiple myeloma (Eligible patients must have quantifiable M-protein levels present in serum and/or urine)
At least 18 years of age.
One or more tumors measurable on radiograph or CT scan, or evaluable disease defined as non-measurable lesions per RECIST or detection of protein M in serum and/or urine of patients with Multiple Myeloma (serum ≥ 10 gm/L and urine ≥ 200 mg/24 hr).
Laboratory data as specified below:
Hematology: ANC >1500 cells/mm3, platelet count >100,000 cells/mm3 and Hemoglobin > 9 gm/L
Hepatic: bilirubin <1.5 X ULN; alanine aminotransferase (ALT) or aspartate aminotransferase (AST) < 2.5 X ULN. Patients with known liver metastases or liver neoplasms: alanine aminotransferase (ALT) or aspartate aminotransferase (AST) < 5.0 X ULN
Renal: serum creatinine within normal limits (WNL), defined as within 10% of the institution's stated reference range, or a calculated creatinine clearance >60 mL/min/1.73 m2 for patients with abnormal, increased, creatinine levels. Patients with Multiple Myeloma (only): serum creatinine ≤ 2.5 the institutional upper limit of the normal range and a calculated creatinine clearance > 40 mL/min/1.73 m2.
Coagulation: INR < 1.5 times normal, aPTT < 1.5 times normal. Patients receiving therapeutic doses of anticoagulant therapy may be considered eligible for the trial if INR and aPTT are within the acceptable therapeutic limits for the institution.
A negative pregnancy test (if female of childbearing potential).
Estimated life expectancy of at least 3 months
Karnofsky Performance Status ≥ 70%
For men and women of child-producing potential, use of effective contraceptive methods during the study
Ability to understand the requirements of the study, provide written informed consent.

Exclusion Criteria:

Pregnant or nursing women.
Seizure disorders requiring anticonvulsant therapy.
Known brain metastases (unless previously treated and well controlled for a period of

or = 3 months).

Major surgery, other than diagnostic surgery, within 4 weeks prior to the first dose of test drug.
Treatment with radiation therapy or surgery within one month prior to study entry
Treatment with chemotherapy or investigational drugs within 21 days prior to the screening visit. Acute toxicities from prior therapy must have resolved to Grade ≤ 1 above baseline.
Patients with a history of a second malignancy within 3 years of the baseline visit excluding cutaneous carcinomas and in-situ carcinoma.
Concurrent severe or uncontrolled medical disease.
Active symptomatic fungal, bacterial and/or viral infection including active HIV or viral hepatitis.
Difficulty with swallowing or an active malabsorption syndrome
Chronic diarrhea
Gastrointestinal diseases including gastritis, ulcerative colitis, Crohn's disease, or hemorrhagic coloproctitis
History of gastric or small bowel surgery involving any extent of gastric or small bowel resection.
Clinically significant bleeding event within the last 3 months, unrelated to trauma, or underlying condition that would be expected to result in a bleeding diathesis
Patients who have exhibited allergic reactions to a similar structural compound or to a formulation component.
Concomitant use of warfarin and HMG-CoA reductase inhibitors (statins)

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Mayo Clinic Arizona	Scottsdale	Arizona	United States	85259
2	Front Range Cancer Specialists	Fort Collins	Colorado	United States	80528
3	Front Range Cancer Specialists	Loveland	Colorado	United States	80528
4	U T M D Anderson Cancer Center	Houston	Texas	United States	77030