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Streptozotocin

Phase 2

Neoplasms | Small molecule | Oncology |Roche Holding AG|Last Updated: Jan 22, 2015

Success Probability

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Market & Valuation

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Trial Design

CONTROLLED
Total Trials1
Total Enrollment83

FDA Designations

No designations recorded

Clinical trial landscape

Streptozotocin · 1 trial · 1 indication

Phase 2 1
NCT00448136A Study of Avastin (Bevacizumab) in Combination With Chemotherapy in Patients With Endocrine Tumors of the Gastrointestinal Tract.Neoplasms
COMPLETED83 Analytics
PHASE2COMPLETED
A Study of Avastin (Bevacizumab) in Combination With Chemotherapy in Patients With Endocrine Tumors of the Gastrointestinal Tract.
NeoplasmsUnlock trial analytics

Study Endpoints

Primary Endpoints

Progression-Free Survival (PFS) - Percentage of Participants With an Event
Screening, every 3 months during treatment, every 6 months during follow-up to 2 years

PFS is defined as the interval between the date of start of treatment and the date of evaluation by the investigator of progressive disease or death from any cause. The progression was assessed according to Response Evaluation Criteria In Solid Tumors (RECIST) using medical imaging during the treatment period and by the investigators (confirmed by medical imaging) during the follow-up period. Data for participants who were lost to follow-up were censored at the date of last evaluation without progression. Data for participants who completed the study without an event of disease progression or death were censored at the date of the last visit or follow-up without progression.

PFS - Time to Event
Screening, every 3 months during treatment, every 6 months during follow-up to 2 years

PFS is defined as the interval between the date of start of treatment and the date of evaluation by the investigator of progressive disease or death from any cause. The progression was assessed according to RECIST using medical imaging during the treatment period and by the investigators (confirmed by medical imaging) during the follow-up period. Data for participants who were lost to follow-up were censored at the date of last evaluation without progression. Data for participants who completed the study without an event of disease progression or death were censored at the date of the last visit or follow-up without progression. Median PFS was estimated using the Kaplan-Meier method.

PFS - Percentage of Participants Estimated to be Progression Free at 12 and 24 Months
Screening, every 3 months during treatment, every 6 months during follow-up to 2 years

PFS is defined as the interval between the date of start of treatment and the date of evaluation by the investigator of progressive disease or death from any cause. The progression was assessed according to RECIST using medical imaging during the treatment period and by the investigators (confirmed by medical imaging) during the follow-up period. Data for participants who were lost to follow-up were censored at the date of last evaluation without progression. Data for participants who completed the study without an event of disease progression or death were censored at the date of the last visit or follow-up without progression.

Secondary Endpoints

Percentage of Participants With a Response by Best Overall Response
Screening, every 3 months during treatment, every 6 months during follow-up to 2 years
Duration of Overall Response (OR) - Percentage of Participants With an Event
Screening, every 3 months during treatment, every 6 months during follow-up to 2 years
Duration of OR - Time to Event
Screening, every 3 months during treatment, every 6 months during follow-up to 2 years
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
1EXPERIMENTAL -
2EXPERIMENTAL -

Interventions

NameTypeDescription
bevacizumab [Avastin]DRUG7.5mg/kg iv on day 1 every 3 weeks
5 FUDRUG400mg/m2/day iv on days 1-5 every 6 weeks
StreptozotocinDRUG500mg/m2/day iv on days 1-5 every 6 weeks
XelodaDRUG1000mg/m2 po bid on days 1-14 every 3 weeks
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites27

Inclusion Criteria: * adult patients, \>=18 years of age; * well-differentiated gastrointestinal tract endocrine tumors, or duodeno-pancreatic endocrine tumors; * no previous anti-cancer therapy, other than surgery; * progressive metastatic disease; * \>=1 measurable lesion. Exclusion Criteria: *...

Countries:France
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Frequently asked questions about Streptozotocin

What is Streptozotocin used for?

Streptozotocin is used for the treatment of neoplasms, which are abnormal growths of tissue that can be benign or malignant. It is being studied in the context of oncology, specifically for endocrine tumors of the gastrointestinal tract, as part of a combination chemotherapy regimen.

What does Streptozotocin target?

Streptozotocin is a small molecule that works by targeting and destroying insulin-producing beta cells in the pancreas. This mechanism makes it useful in treating certain types of pancreatic tumors, particularly those that arise from these cells, such as insulinomas.

Who makes Streptozotocin?

Streptozotocin is being developed by Roche Holding AG, a multinational healthcare company. The company's stock is traded under the ticker symbol RHHBY on the OTC market.

What phase is Streptozotocin in?

Streptozotocin is currently in Phase 2 clinical development. It is an investigational drug and has not yet been approved by regulatory authorities. One Phase 2 trial has been completed, with no active trials currently ongoing.

What clinical trials is Streptozotocin in?

Streptozotocin was studied in a completed Phase 2 clinical trial with the identifier NCT00448136. This trial, titled 'A Study of Avastin (Bevacizumab) in Combination With Chemotherapy in Patients With Endocrine Tumors of the Gastrointestinal Tract,' enrolled 83 participants in France.

Is Streptozotocin the same as other drugs?

Streptozotocin is a distinct chemical compound and is not known to be the same as other drugs. It is a small molecule with a unique structure that specifically targets pancreatic beta cells, making it different from other chemotherapy agents.