Clinical Trials Logo

Clinical Trial Summary

Participants will take GW572016 by mouth daily each cycle (cycles 28 days in length) and will be given Topotecan intravenously on Days 1, 8 and 15.


Clinical Trial Description

Participants will take GW572016 by mouth daily each cycle (cycles 28 days in length) and will be given Topotecan intravenously on Days 1, 8 and 15. During Cycle 1 participants will be required to spend the evening before Day 1 in the General Clinical Research Center and frequent blood samples will be drawn on Day 1; this schedule will be repeated the evening of Day 6 with the blood samples drawn on Day 7. Participants will have weekly CBCs. ;


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00295243
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase Phase 1
Start date September 2004
Completion date November 2006

See also
  Status Clinical Trial Phase
Terminated NCT02080078 - A Phase I Dose Escalation Study of Erlotinib in Combination With Theophylline Phase 1
Completed NCT00981721 - A Study to Determine the Pharmacokinetics of Cediranib in Chinese Patients With Advanced Solid Malignancies Phase 1
Terminated NCT00351325 - A Study of BMS-663513 Administered in Combination With Chemotherapy to Subjects With Advanced Solid Malignancies Phase 1
Recruiting NCT02347228 - Evaluate Safety, Tolerability, PK, Preliminary Clinical Activity of OB318 in Patients With Advanced Solid Malignancies Phase 1
Terminated NCT00979134 - Study is Designed to Assess the Safety and Tolerability of AZD4547 at Increasing Doses in Patients With Advanced Tumours Phase 1
Completed NCT00997945 - 10mg ZD4054 (Zibotentan) PK Study in Male, Elderly Chinese Patients With Advanced Solid Malignancies Phase 1
Active, not recruiting NCT05573724 - Drug-drug Interaction Study With AZD5305 and Itraconazole in Patients With Advanced Solid Malignancies Phase 1
Completed NCT03736473 - A Phase I Study of MEDI9447 (Oleclumab) in Japanese Patients Phase 1
Completed NCT02260661 - Phase I, Dose Study to Look at the Safety and Pharmacokinetics of AZD8835 in Patients With Advanced Solid Tumours Phase 1
Completed NCT01213160 - Study to Assess Safety and Tolerability of AZD4547 in Japanese Patient Phase 1
Terminated NCT01219543 - A Phase I Study of AZD1480 in Patients With Advanced Solid Malignancies and Advanced Hepatocellular Carcinoma in the Escalation Phase,Non-Small Cell Lung Cancer(NSCLC) and Non-smokers With Lung Metastasis and Gastric Cancer and Solid Tumour in the Expansion Phase. Phase 1
Completed NCT00572364 - Open Label, Dose Escalation Phase I Study of AZD2281 Phase 1
Completed NCT03363893 - Modular Study to Evaluate CT7001 Alone in Cancer Patients With Advanced Malignancies Phase 1/Phase 2
Recruiting NCT04606381 - A Study of Amivantamab Subcutaneous (SC) Administration for the Treatment of Advanced Solid Malignancies Phase 1
Recruiting NCT05315167 - A Phase I/II Study to Evaluate the Safety, Pharmacokinetics and Efficacy of PRJ1-3024 in Subjects With Advanced Solid Tumors Phase 1/Phase 2
Completed NCT00879905 - A Study of HSP990 Administered by Mouth in Adult Patients With Advanced Solid Tumors Phase 1
Terminated NCT00473616 - Phase I Single Ascending Dose/Multiple Ascending Dose in Patients Treated With AZD7762 and Irinotecan Phase 1
Recruiting NCT05159700 - A Phase I Study, Evaluating the Safety, Pharmacokinetics and Efficacy of PRJ1-3024 in Subjects With Advanced Solid Tumors Phase 1
Completed NCT01813474 - Investigate the Safety and Tolerability of Olaparib Tablet in Japanese Patients With Advanced Solid Malignancies Phase 1
Completed NCT01102400 - A Study of MEDI-575 in Patients With Advanced Solid Malignancies Phase 1