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A Phase I Dose-Escalation Study of NMS-1116354 in Adult Patients With Advanced Solid Tumors


Phase 1
18 Years
80 Years
Not Enrolling
Both
Advanced Solid Tumors

Thank you

Trial Information

A Phase I Dose-Escalation Study of NMS-1116354 in Adult Patients With Advanced Solid Tumors


Inclusion Criteria:



1. Advanced/metastatic solid tumors, for which no alternative effective standard therapy
is available

2. Maximum of 4 regimens of prior cancer therapy allowed

3. Prior radiotherapy allowed if no more than 25% of BM reserve irradiated

4. Resolution of all acute toxic effects (excluding alopecia) of any prior anticancer
therapy

5. ECOG performance status (PS) 0 or 1

6. Adult (age >/= 18 and
7. Adequate renal, liver and BM reserve

8. Capability to swallow capsules intact

Exclusion Criteria:

1. Current enrollment in another therapeutic clinical trial

2. Known brain metastases

3. Currently active second malignancy

4. Major surgery within 4 weeks prior to treatment

5. Any of the following in the past 6 months: myocardial infarction, unstable angina,
coronary/peripheral artery bypass graft, symptomatic congestive heart failure,
cerebrovascular accident or transient ischemic attack, pulmonary embolism, deep vein
thrombosis

6. Pregnancy or breast-feeding women

7. Known active infections

8. Gastrointestinal disease or other malabsorption syndromes that would impact on drug
absorption

9. Adrenal insufficiency

10. Other severe acute or chronic medical or psychiatric condition that could compromise
protocol objectives

Type of Study:

Interventional

Study Design:

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

First cycle dose-limiting toxicities (DLTs) and related maximum tolerated dose (MTD)

Outcome Time Frame:

Cycle 1

Safety Issue:

Yes

Principal Investigator

Kyriakos Papadopoulos, MD, MSc

Investigator Role:

Principal Investigator

Investigator Affiliation:

South Texas Accelerated Research Therapeutics (START)

Authority:

United States: Food and Drug Administration

Study ID:

CDCA-354-001

NCT ID:

NCT01016327

Start Date:

April 2009

Completion Date:

September 2012

Related Keywords:

  • Advanced Solid Tumors
  • Phase I study
  • Advanced Solid Tumors
  • Cdc7 kinase inhibitor
  • Neoplasms

Name

Location

South Texas Accelerated Research Therapeutics (START) San Antonio, Texas  78229