Gem-TABS in Unresectable Pancreatic Carcinoma
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|ClinicalTrials.gov Identifier: NCT01198821|
Recruitment Status : Completed
First Posted : September 10, 2010
Last Update Posted : February 23, 2017
The purpose of this study is to:
Find out the largest dose of sodium bicarbonate that can be given with gemcitabine.
Determine if the combination of sodium bicarbonate and gemcitabine produces better control of pancreatic cancer than gemcitabine alone.
|Condition or disease||Intervention/treatment||Phase|
|Pancreatic Cancer||Drug: Sodium bicarbonate (g/kg/day) Drug: Gemcitabine (mg/m²)||Phase 1|
Gemcitabine will be administered as an intravenous drip over 30 minutes at a dose of 1000 mg/m2 on days 1, 8, and 15 of each cycle followed by a 7-day treatment rest period. No treatment will be administered on the 4th week of the cycle. Each cycle is 28 days long.
Sodium bicarbonate is commercially available and supplied as tablets and water soluble powder. It is stable in solid form and does not need refrigeration. The sodium bicarbonate will be dispensed by the pharmacy in packets containing 1/3 the daily dose. The patient will be asked to dissolve the powder in water 3 times per day and consume the dose over a period of about 30 minutes.
Patients will be required to refrain from use of additional buffering agents (antacids) including sodium bicarbonate, CaCO3, and aluminum hydroxide.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||8 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase I Study of Oral Sodium Bicarbonate in Patients With Unresectable Pancreatic Carcinoma Treated With Gemcitabine|
|Study Start Date :||August 2010|
|Actual Primary Completion Date :||June 2011|
|Actual Study Completion Date :||June 2011|
|Experimental: Oral sodium bicarbonate and Gemcitabine||
Drug: Sodium bicarbonate (g/kg/day)
Dose Escalation - Level 1: 0.3, Level 2: 0.5, Level 3: 0/7, Level 4: 1.0
Drug: Gemcitabine (mg/m²)
Dose Escalation - Level 1: 1000, Level 2: 1000, Level 3: 1000, Level 4: 1000
- Establish the safety and tolerability of oral sodium bicarbonate in patients with advanced pancreatic carcinoma treated with gemcitabine [ Time Frame: Average of 6 months ]
- Determine if oral bicarbonate improves overall survival, progression free-survival and response rate in patients with advanced pancreatic cancer [ Time Frame: Average of 6 months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01198821
|United States, Florida|
|H. Lee Moffitt Cancer Center and Research Institute|
|Tampa, Florida, United States, 33612|
|Principal Investigator:||Gregory Springett, M.D., Ph.D.||H. Lee Moffitt Cancer Center and Research Institute|