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Study of Cryoablation and Nirogacestat for Desmoid Tumor
Recruiting
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The primary purpose of this protocol is Systemic therapy with oral study agent, nirogacestat,
followed by a single cryoablation procedure.
Lead Sponsor
Stanford Investigators
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A Study of Unesbulin in Participants With Advanced Leiomyosarcoma (LMS)
Not Recruiting
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This study will compare the efficacy and safety of unesbulin plus dacarbazine versus placebo
plus dacarbazine in participants with unresectable or metastatic, relapsed or refractory LMS
who have received at least 1 prior line of systemic therapy.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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Phase 2 Basket Trial of Nab-sirolimus in Patients With Malignant Solid Tumors With Pathogenic Alterations in TSC1/TSC2 Genes (PRECISION 1)
Recruiting
More
A Phase 2 multi-center open-label basket trial of nab-sirolimus for adult and adolescent
patients with malignant solid tumors harboring pathogenic inactivating alterations in TSC1 or
TSC2 genes
Stanford Investigators
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Adoptive Cell Therapy Long-term Follow-up (LTFU) Study
Not Recruiting
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This trial will evaluate long term safety of participants who have received GlaxoSmithKline
(GSK) adoptive cell therapy for up to 15 years following last adoptive cell therapy infusion.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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ENVASARC: Envafolimab And Envafolimab With Ipilimumab In Patients With Undifferentiated Pleomorphic Sarcoma Or Myxofibrosarcoma
Recruiting
More
This is a multicenter open-label, randomized, non-comparative, parallel cohort pivotal study
of treatment with envafolimab (cohort A and C) or envafolimab combined with ipilimumab
(cohort B and D) in patients with locally advanced, unresectable or metastatic
undifferentiated pleomorphic sarcoma (UPS)/myxofibrosarcoma (MFS) who have progressed on one
or two lines of chemotherapy.
Stanford Investigators
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18F-FTC-146 PET/CT in Newly-Diagnosed Osteosarcoma
Not Recruiting
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The purpose of this research is to evaluate the study drug, 18F FTC-146, as a positron
emission tomography (PET) / computed tomography (CT) radiotracer imaging agent to evaluate
tumor status in patients newly diagnosed with osteosarcoma ("bone cancer").
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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CytoreductiveSurgery & HIPEC w/Gemcitabine+Chemotherapy w/Dacarbazine in Uterine Leiomyosarcoma
Not Recruiting
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The purpose of this study is to find out if giving a dose of heated chemotherapy in the
abdomen immediately after surgery that is done to remove uterine leiomyosarcoma type of
cancer will help lower the risk of the cancer coming back in the future.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-725-6413.
Stanford Investigators
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Master Protocol to Assess the Safety and Antitumor Activity of Genetically Engineered T Cells in NY-ESO-1 and/or LAGE-1a Positive Solid Tumors
Not Recruiting
More
This trial will evaluate safety and efficacy of human engineered T-cell therapies, in
participants with advanced tumors.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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Study of DCC-3014 in Patients With Advanced Tumors and Tenosynovial Giant Cell Tumor
Recruiting
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This is a multicenter, open-label Phase 1/2 study of DCC-3014 in patients with malignant
solid tumors and tenosynovial giant cell tumor (TGCT). There will be 2 distinct parts in this
study: Dose Escalation (Phase 1) and Expansion (Phase 2). Phase 1 will enroll both malignant
solid tumor and TGCT patients. Phase 2 will comprise two cohorts (Cohort A and Cohort B) and
will only enroll TGCT patients.
Stanford Investigators
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Cabozantinib Combined With PD-1 and CTLA-4 Inhibition in Metastatic Soft Tissue Sarcoma
Not Recruiting
More
The hypothesis of this study is that the response rate of soft tissue sarcoma will be
improved with the addition of PD-1 and CTLA-4 inhibition to cabozantinib, and that
cabozantinib priming will increase the response to nivolumab and ipilimumab.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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Ipilimumab + Nivolumab + Cryotherapy in Metastatic or Locally Advanced Soft Tissue Sarcoma
Not Recruiting
More
The purpose of this Phase 2 study is to
1. find out if the study drugs (ipilimumab plus nivolumab) in combination with cryotherapy
will help participants with metastatic or locally advanced soft tissue sarcoma;.
2. find out how safe are ipilimumab plus nivolumab given in combination with cryotherapy,
and what side effects may be related to treatment.
3. find out how do the study drugs in combination with cryotherapy work in soft tissue
sarcoma.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-498-7061.
Stanford Investigators
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Expanded Access for ABI-009 in Patients With Advanced PEComa and Patients With a Malignancy With Relevant Genetic Mutations or mTOR Pathway Activation
Not Recruiting
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Expanded Access for an Intermediate-size Population for ABI-009 (Sirolimus Albumin-bound
Nanoparticles for Injectable Suspension) in Patients with Advanced Perivascular Epithelioid
Cell Tumors (PEComa) and Patients with a Malignancy with Relevant Genetic Mutations or mTOR
Pathway Activation
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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A Study of Ripretinib vs Sunitinib in Advanced GIST Patients After Treatment With Imatinib
Not Recruiting
More
This is a 2-arm, randomized, open-label, international, multicenter study comparing the
efficacy of ripretinib to sunitinib in GIST patients who progressed on or were intolerant to
first-line anticancer treatment with imatinib. Approximately 426 patients will be randomized
in a 1:1 ratio to ripretinib 150 mg once daily (continuous dosing for 6 week cycles) or
sunitinib 50 mg once daily (6 week cycles, 4 weeks on, 2 weeks off).
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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ADI-PEG 20 in Combination With Gemcitabine and Docetaxel for the Treatment of Soft Tissue Sarcoma, Osteosarcoma, Ewing's Sarcoma, and Small Cell Lung Cancer
Not Recruiting
More
The investigators have recently demonstrated that argininosuccinate synthase 1 (ASS1)
expression is silenced in 88% of all sarcomas (n=708), and that this loss is associated with
a decreased overall survival. Using the extracellular arginine depleting enzyme PEGylated
arginine deiminase (ADI-PEG20), an extracellular arginine depleting enzyme, the investigators
demonstrated ADI-PEG20 induces a prosurvival metabolic reprogramming in ASS1-deficient
sarcomas that redirects glucose into the serine/folate pathway directing the carbons from
glucose into pyrimidine biosynthesis, thus sensitizing cells to death by the pyrimidine
antimetabolite gemcitabine by using metabolomics. The synthetic lethality was increased by
the addition of docetaxel. Therefore a phase II clinical trial of ADI with gemcitabine and
docetaxel, a standard second line therapy for soft tissue sarcoma will be conducted to
determine if the clinical benefit rate of gemcitabine and docetaxel is improved by the
metabolic changes induced by ADI-PEG20.
Recently published data shows that priming ASS1-deficient tumors with ADI-PEG 20 and
docetaxel improves the effect of gemcitabine. Therefore, a cohort of patients consisting of
ten patients diagnosed with either osteosarcoma or Ewing's sarcoma (ideally five of each),
and five patients diagnosed with small cell lung cancer will be included as an exploratory
cohort. Enrollment to Cohort 2 will occur concurrently with Cohort 1.
Stanford is currently not accepting patients for this trial.
For more information, please contact Nam Bui, M.D., 713-412-8721.
Stanford Investigators
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Spearhead 1 Study in Subjects With Advanced Synovial Sarcoma or Myxoid/Round Cell Liposarcoma
Recruiting
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This is a study to investigate the efficacy and safety of ADP-A2M4 in HLA-A*02 eligible and
MAGE-A4 positive subjects with metastatic or inoperable (advanced) Synovial Sarcoma (Cohort
1, 2 and 3 ) or MRCLS (Cohort 1) .
Stanford Investigators
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Trametinib in Treating Patients With Epithelioid Hemangioendothelioma That is Metastatic, Locally Advanced, or Cannot Be Removed by Surgery
Not Recruiting
More
This phase II trial studies how well trametinib works in treating patients with epithelioid
hemangioendothelioma that has spread to other places in the body (metastatic), nearby tissue
or lymph nodes (locally advanced), or cannot be removed by surgery (unresectable). Trametinib
may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.
Stanford is currently not accepting patients for this trial.
For more information, please contact Kristen N. Ganjoo, 650-498-7061.
Stanford Investigators
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Cabozantinib for Adults With Advanced Soft Tissue Sarcoma
Not Recruiting
More
Background:
- Cabozantinib is a cancer treatment drug that blocks the growth of new blood vessels in
tumors. It can also block a chemical on tumor cells that allows the cells to grow. A similar
drug, pazopanib, is used to treat types of cancer known as sarcomas. Researchers want to see
if cabozantinib can be an effective treatment for types of soft tissue sarcoma that have not
responded to earlier treatments.
Objectives:
- To test the effectiveness of cabozantinib for soft tissue sarcomas that have not responded
to standard treatments.
Eligibility:
- Individuals at least 18 years of age who have soft tissue sarcomas that have not responded
to standard treatments.
Design:
- Participants will be screened with a physical exam and medical history. Blood samples
will be collected. Imaging studies and other tests will be used to study the tumor
before the start of treatment.
- Participants will take cabozantinib tablets daily for 28-day cycles of treatment. The
tablets should be taken whole on an empty stomach.
- Treatment will be monitored with frequent blood tests and imaging studies.
- Participants will continue to take cabozantinib for as long as the tumor does not become
worse and the side effects are not too severe.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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Phase 3 Study of DCC-2618 vs Placebo in Advanced GIST Patients Who Have Been Treated With Prior Anticancer Therapies
Not Recruiting
More
This is a 2-arm, randomized, placebo-controlled, double-blind, international, multicenter
study comparing the efficacy of ripretinib (DCC-2618) to placebo in patients who have
received treatment with prior anticancer therapies. Prior anticancer therapies must include
imatinib, sunitinib, and regorafenib (3 prior therapies). Approximately 120 patients were
randomized in a 2:1 ratio to ripretinib 150 mg QD or placebo
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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Trial of TRC105 and Pazopanib Versus Pazopanib Alone in Patients With Advanced Angiosarcoma
Not Recruiting
More
This is a study of TRC105 in combination with standard dose pazopanib compared to single
agent pazopanib in patients with angiosarcoma not amenable to curative intent surgery (e.g.,
metastatic or bulky disease, and disease for which surgical resection would carry an
unacceptable risk to the patient) who have not received pazopanib or TRC105 previously.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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A Study of Atezolizumab Plus Cobimetinib and Vemurafenib Versus Placebo Plus Cobimetinib and Vemurafenib in Previously Untreated BRAFv600 Mutation-Positive Patients With Metastatic or Unresectable Locally Advanced Melanoma
Not Recruiting
More
This is a Phase III, double-blinded, placebo-controlled, randomized, multicenter study
designed to evaluate the efficacy, safety, and pharmacokinetics of atezolizumab + cobimetinib
+ vemurafenib compared with placebo + cobimetinib + vemurafenib in patients with previously
untreated BRAFv600 mutation-positive metastatic or unresectable locally advanced melanoma.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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Paclitaxel + Bevacizumab (Avastin) for the Treatment of Metastatic or Unresectable Angiosarcoma
Not Recruiting
More
This is an open-label, single-arm, multi-center, Phase 2 study with Paclitaxel in combination
with Bevacizumab in patients with Unresectable or Metastatic Angiosarcoma. The study aims to
determine the safety and effectiveness of combining two drugs Paclitaxel and Bevacizumab in
the treatment of Angiosarcoma that cannot be removed by surgery, or has spread to other parts
of your body. The primary objective is to evaluate 4month non progression rate. The secondary
objective is to evaluate overall response rate after 3rd and 6th cycle, median duration of
response, 6th and 12th month survival, toxicity of Paclitaxel and Bevacizumab combination,
toxicity of maintenance Bevacizumab and to collect paraffin-embedded tumor blocks for
angiogenesis markers and tissue microarray.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-725-6413.
Lead Sponsor
Stanford Investigators
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Safety Study of MGD009 in B7-H3-expressing Tumors
Not Recruiting
More
The purpose of this study is to evaluate the safety of MGD009 when given to patients with
B7-H3-expressing tumors. The study will also evaluate what is the highest dose of MGD009 that
can be given safely. Assessments will be done to see how the drug acts in the body
(pharmacokinetics (PK), pharmacodynamics (PD) and to evaluate potential anti-tumor activity
of MGD009.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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Selinexor in Advanced Liposarcoma
Not Recruiting
More
This is a randomized, multicenter, double-blind, placebo-controlled, Phase 2-3 study of
patients diagnosed with advanced unresectable dedifferentiated liposarcoma. Approximately 342
total patients will be randomized to study treatment (selinexor or placebo).
Stanford is currently not accepting patients for this trial.
For more information, please contact Kristen Ganjoo, MD, .
Stanford Investigators
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Effect of Pexidartinib on the Way the Body Processes CYP3A4 and CYP2C9 Substrates (Pharmacokinetics)
Not Recruiting
More
This study has two parts.
Part 1 will evaluate how pexidartinib affects the way the body processes CYP3A4 and CYP2C9
substrates using midazolam and tolbutamide, respectively, as probe agents.
Part 2 will test the efficacy and safety of pexidartinib treatment in various tumor types.
In Part 2, the same participants will continue to receive pexidartinib twice daily.
Participants will be allowed to continue using pexidartinib as long as the participant
derives benefit.
Stanford is currently not accepting patients for this trial.
For more information, please contact Site Coordinator, 650-723-2868.
Stanford Investigators
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Efficacy and Safety Study of CC-4047 (Pomalidomide) to Treat Advanced Soft Tissue Sarcoma
Not Recruiting
More
The purpose of the study is to determine the safety and efficacy of single agent CC-4047
(pomalidomide) in patients with advanced soft tissue sarcomas who have relapsed or are
refractory to prior anticancer therapy.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 6507256413.
Stanford Investigators
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Nilotinib in Patients With Relapsed or Metastatic Pigmented Villonodular Synovitis/Tenosynovial Giant Cell Tumor/Diffuse-Type Giant Cell Tumor
Not Recruiting
More
Nilotinib is a drug that is used to treat a form of a blood cancer called leukemia. Nilotinib
works by blocking the action of a protein that might be important for the growth of pigmented
villonodular synovitis (PVNS). In this research study the investigators are testing whether
nilotinib can stop the growth of PVNS or improve the symptoms experienced from PVNS.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 6507256413.
Stanford Investigators
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A Safety, Tolerability and PK Study of DCC-2618 in Patients With Advanced Malignancies
Not Recruiting
More
This is a Phase 1, open-label, first-in-human (FIH) dose-escalation study designed to
evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and
preliminary antitumor activity of DCC-2618, administered orally (PO), in adult patients with
advanced malignancies. The study consists of 2 parts, a dose-escalation phase, and an
expansion phase. All active patients (from both dose-escalation and expansion phases) will
then transition into an extension phase.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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A Phase 2 Study of Nab-sirolimus (ABI-009) in Patients With Advanced Malignant PEComa
Not Recruiting
More
A phase 2 multi-center investigation of efficacy of nab-sirolimus (formerly known as ABI-009
or nab-rapamycin) in patients with advanced malignant perivascular epithelioid cell tumor
(PEComa).
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-725-6413.
Stanford Investigators
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Study to Compare the Safety and Efficacy of CMB305 With Atezolizumab to Atezolizumab Alone in Participants With Sarcoma (IMDZ-C232/V943A-002)
Not Recruiting
More
This is an open-label Phase 2 randomized study that will examine the use of the study agents,
CMB305 (sequentially administered LV305 which is a dendritic cell-targeting viral vector
expressing the New York Esophageal Squamous Cell Carcinoma 1 gene [NY-ESO-1] and G305 which
is a NY-ESO-1 recombinant protein plus glucopyranosyl lipid adjuvant-stable emulsion
[GLA-SE]) in combination with atezolizumab or atezolizumab alone, in participants with
locally advanced, relapsed or metastatic sarcoma (synovial or myxoid/round cell liposarcoma)
expressing the NY-ESO-1 protein.
There is no formal primary hypothesis for this study.
Stanford is currently not accepting patients for this trial.
For more information, please contact Cancer Clinical Trials Office (CCTO), 650-498-7061.
Stanford Investigators
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A Study of Doxorubicin Plus Olaratumab (LY3012207) in Participants With Advanced or Metastatic Soft Tissue Sarcoma
Not Recruiting
More
The main purpose of this study is to evaluate the efficacy of the combination of doxorubicin
plus the study drug known as olaratumab versus doxorubicin plus placebo in participants with
advanced or metastatic soft tissue sarcoma.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-725-6413.
Stanford Investigators
View full details
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Study of Cabiralizumab in Patients With Pigmented Villonodular Synovitis / Diffuse Type Tenosynovial Giant Cell Tumor
Not Recruiting
More
This is a phase 1/2 single arm, open-label, safety, tolerability, and PK study of
cabiralizumab in PVNS/dt-TGCT patients.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-725-6413.
Stanford Investigators
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Phase 3 Study to Treat Patients With Soft Tissue Sarcomas
Not Recruiting
More
The purpose of this study is to determine the efficacy and safety of aldoxorubicin in
subjects with metastatic, locally advanced, or unresectable soft tissue sarcomas.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-725-6413.
Stanford Investigators
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Phase 3 Study of Pexidartinib for Pigmented Villonodular Synovitis (PVNS) or Giant Cell Tumor of the Tendon Sheath (GCT-TS)
Not Recruiting
More
This is a Phase 3 clinical study, which aims to evaluate the effectiveness of an
investigational drug called pexidartinib for the treatment of certain tumors for which
surgical removal could cause more harm than good.
The main purpose of this study is to gather information about the investigational drug
pexidartinib, which may help to treat tumors of pigmented villonodular synovitis (PVNS) or
giant cell tumor of the tendon sheath (GCT-TS).
The study consists of two parts with a follow-up period. In Part 1, eligible study
participants will be assigned to receive either pexidartinib or matching placebo for 24
weeks. A number of assessments will be carried out during the course of the study, including
physical examinations, blood tests, imaging studies, electrocardiograms, and questionnaires.
MRI scans will be used to evaluate the response of the tumors to the treatment. Some
subjects, assigned to placebo in Part 1 transitioned to pexidartinib for Part 2.
Then a protocol amendment was written to allow only pexidartinib patients to continue into
Part 2. Part 2 is a long-term treatment phase in which all participants receive open-label
pexidartinib. There was also a follow-up period added to Part 2.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-725-6413.
Stanford Investigators
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SARC024: A Blanket Protocol to Study Oral Regorafenib in Patients With Selected Sarcoma Subtypes
Not Recruiting
More
Although regorafenib was approved for use in patients who had progressive GIST despite
imatinib and/or sunitinib on the basis of phase II and phase III data, it has not been
examined in a systematic fashion in patients with other forms of sarcoma.
Given the activity of sorafenib, sunitinib and pazopanib in soft tissue sarcomas, and
evidence of activity of sorafenib in osteogenic sarcoma and possibly Ewing/Ewing-like
sarcoma, there is precedent to examine SMOKIs (small molecule oral kinase inhibitors) such as
regorafenib in sarcomas other than GIST. It is also recognized that SMOKIs (small molecule
oral kinase inhibitors)such as regorafenib, sorafenib, pazopanib, and sunitinib have
overlapping panels of kinases that are inhibited simultaneously. While not equivalent, most
of these SMOKIs (small molecule oral kinase inhibitors) block vascular endothelial growth
factor and platelet derived growth factors receptors (VEGFRs and PDGFRs), speaking to a
common mechanism of action of several of these agents.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-725-6413.
Stanford Investigators
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A Trial of TH-302 in Combination With Doxorubicin Versus Doxorubicin Alone to Treat Patients With Locally Advanced Unresectable or Metastatic Soft Tissue Sarcoma
Not Recruiting
More
The purpose of this study is to determine whether TH-302 in combination with Doxorubicin is
safe and effective in the treatment of Locally Advanced Unresectable or Metastatic Soft
Tissue Sarcoma.
Stanford is currently not accepting patients for this trial.
For more information, please contact John Ramirez, 6507230387.
Stanford Investigators
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Linsitinib in Treating Patients With Gastrointestinal Stromal Tumors
Not Recruiting
More
This phase II trial studies how well linsitinib works in treating younger and adult patients
with gastrointestinal stromal tumors. Linsitinib may stop the growth of tumor cells by
blocking some of the enzymes needed for cell growth.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 650-725-6413.
Stanford Investigators
View full details
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Preliminary Efficacy and Safety of INNO-206 Compared to Doxorubicin in Advanced Soft Tissue Sarcoma
Not Recruiting
More
This is a phase 2b, randomized, open-label, prospective, multicenter study comparing
treatment with INNO 206 to doxorubicin in subjects with metastatic, locally advanced, or
unresectable soft tissue sarcomas who have not been previously treated with any chemotherapy
except potentially as adjuvant or neoadjuvant chemotherapy, and no evidence of tumor
recurrence has occurred for at least 12 months.
Stanford is currently not accepting patients for this trial.
For more information, please contact Catherine Norton, 650-723-2868.
Stanford Investigators
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A Study of Trabectedin or Dacarbazine for the Treatment of Patients With Advanced Liposarcoma or Leiomyosarcoma
Not Recruiting
More
The purpose of this study is to evaluate whether overall survival for the trabectedin group
is superior to the dacarbazine group for patients with advanced L-sarcoma (liposarcoma or
leiomyosarcoma).
Stanford is currently not accepting patients for this trial.
For more information, please contact Catherine Norton, 650723-2868.
Stanford Investigators
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Phase 3 Study to Compare the Efficacy and Safety of Eribulin With Dacarbazine in Subjects With Soft Tissue Sarcoma
Not Recruiting
More
This is a randomized, open-label, multicenter, Phase 3 study comparing the efficacy and
safety of eribulin with dacarbazine in subjects with advanced soft tissue sarcoma who have
disease progression within 6 months prior to study enrolment following standard therapies
which must have included an anthracycline, unless contraindicated and then at least one
additional regimen after failure of the anthracycline.
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 6507256413.
Stanford Investigators
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Pazopanib in Imatinib Refractory or Intolerant Gastrointestinal Stromal Tumors (GIST)
Not Recruiting
More
This study is being done to gather information about the safety (any harmful effects) and
effectiveness (usefulness) of Pazopanib in the treatment of Gastrointestinal Stroma Tumors
(GIST) that cannot be treated by surgery or has spread to other organs. The Food and Drug
Administration (FDA) have approved Pazopanib for the treatment of advanced kidney cancer but
it is not approved for the treatment of GIST. The investigators hope to learn about the
safety and usefulness (effectiveness) of Pazopanib for patients with GIST.
Primary Objective:
Non-progression rate based on RECIST criteria (CR+PR+SD)
Secondary Objectives:
- Response per Choi criteria
- 6 month progression-free survival
- Safety and tolerability
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahern, 6507256413.
Stanford Investigators
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Study of Denosumab in Subjects With Giant Cell Tumor of Bone
Not Recruiting
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To determine how safe denosumab is in treating subjects with giant cell tumor of bone (GCTB)
Stanford is currently not accepting patients for this trial.
For more information, please contact Maria Ahem, 6507256413.
Stanford Investigators
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