Know Cancer

or
forgot password

A Phase I Study of MK8669 in Patients With Metastatic or Locally Advanced Solid Tumors


Phase 1
20 Years
N/A
Not Enrolling
Both
Neoplasm

Thank you

Trial Information

A Phase I Study of MK8669 in Patients With Metastatic or Locally Advanced Solid Tumors


Inclusion Criteria:



- Histologically - Or Cytologically- Confirmed Metastatic Or Locally Advanced Solid
Tumors That Has Failed To Respond To Standard Therapy, Or For Which Adequate Standard
Therapy Dose Not Exist

- ECOG Performance Status 0 or 1

- Adequate Organ Function

Exclusion Criteria:

- Patient Who Has Had Chemotherapy, Radiotherapy, Or Biological Therapy Within 4 Weeks
(6 Weeks For Nitrosoureas Or Mitomycin C) Prior To Registration

- Any CNS Metastasis Which Has Symptom Or Requires Treatment

- Any Primary Central Nervous System Tumor

- Any Symptomatic Ascites Or Plural Effusion Which Requires Treatment

- A History Or Current Evidence Of Any Clinically Significant Disease That Might
Confound The Results Of The Study, Complicate The Interpretation Of The Study
Results, Interfere With The Patient'S Participation, Or Pose An Additional Risk To
The Patient

Type of Study:

Interventional

Study Design:

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

Outcome Measure:

Any clinical or laboratory adverse experience.

Outcome Time Frame:

Duration of Treatment

Safety Issue:

Yes

Principal Investigator

Medical Monitor

Investigator Role:

Study Director

Investigator Affiliation:

Merck

Authority:

Japan: Pharmaceuticals and Medical Devices Agency

Study ID:

2008_011

NCT ID:

NCT00694083

Start Date:

June 2008

Completion Date:

September 2009

Related Keywords:

  • Neoplasm
  • Neoplasms

Name

Location