CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Standard Dose BevacizumabWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug2397 Reduced Dose Bevacizumab Wiki 1.00
drug1883 Nivolumab Wiki 0.58

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D005909 Glioblastoma NIH 0.71

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0012174 Glioblastoma multiforme HPO 0.71

There is one clinical trial.

Clinical Trials


1 CA209-382 A Randomized Phase 2 Open Label Study of Nivolumab Plus Standard Dose Bevacizumab Versus Nivolumab Plus Low Dose Bevacizumab in Recurrent Glioblastoma (GBM)

The purpose of this study is to test the effectiveness (how well the drug works), safety and tolerability of an investigational drug called nivolumab (also known as BMS-936558) in glioblastoma (a malignant tumor, or GBM), when added to bevacizumab. Nivolumab is an antibody (a kind of human protein) that is being tested to see if it will allow the body's immune system to work against glioblastoma tumors. Opdivo (Nivolumab) is currently FDA approved in the United States for melanoma (a type of skin cancer), non-small cell lung cancer, renal cell cancer (a type of kidney cancer), Hodgkin's lymphoma but is not approved in glioblastoma. Nivolumab may help your immune system detect and attack cancer cells. Bevacizumab is a drug which works on the blood vessel that supply the tumor and potentially can starve the tumor by cutting off the blood supply to these tumors. Bevacizumab is commercially available and FDA approved for patients with recurrent glioblastoma. This study has two study groups. Arm 1 will receive the study drug Nivolumab 240mg and bevacizumab 10 mg (standard dose) every 2 weeks and Arm 2 will receive the study drug Nivolumab 240 mg and bevacizumab 3 mg (reduced dose) every 2 weeks. A process will be used to assign patients, by chance, to one of the study groups. Neither patients nor doctors can choose which group patients are in. This is done by chance because no one knows if one study group is better or worse than the other. 90 total patients are expected to participate in this study (45 patients in each arm). Your total participation in this study from the time you have signed the informed consent to your last visit, including follow-up visits, may be more than three years (depending on what effect the treatment has on your cancer, and how well you tolerate the treatment).

NCT03452579 Glioblastoma Drug: Nivolumab Drug: Standard Dose Bevacizumab Drug: Reduced Dose Bevacizumab
MeSH:Glioblastoma
HPO:Glioblastoma multiforme

Primary Outcomes

Description: The proportion of subjects in the analysis population who remain alive for at least twelve months following initiation of study therapy.

Measure: Overall Survival at 12 Months

Time: Up to 12 months after beginning therapy

Secondary Outcomes

Description: Time from beginning of treatment to death

Measure: Overall Survival

Time: Up to 3 years after beginning treatment

Description: Proportion of subjects in the analysis population who have complete response (CR) or partial response (PR) using Radiologic Assessment in Neuro-Oncology criteria (RANO) criteria.

Measure: Overall Response Rate

Time: Up to 3 years after beginning treatment

Description: Time from first RANO response to disease progression in subjects who achieve a PR or better

Measure: Duration of Response

Time: Up to 3 years after beginning treatment

Description: Defined as the time from allocation to the first documented disease progression according to RANO or death due to any cause, whichever occurs first

Measure: Progression-Free Survival

Time: Up to 3 years after beginning treatment

Description: The proportion of subjects in the analysis population who remain progression-free for at least six months following initiation of study therapy

Measure: Progression-Free Survival at Six Months

Time: Up to six months after beginning treatment


Related HPO nodes (Using clinical trials)