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Clinical Trial Finder

Search Results

Meclofenamate in Subjects With Recurrent or Progressive Brain Metastasis From Solid Tumor Primary

Study Purpose

Cancer that has spread to the brain, or brain metastasis, is difficult to treat. Meclofenamate is a drug which has been shown to reduce brain metastasis growth in the laboratory. This medicine has been used in the past to treat pain. But, in this study, it will be used to prevent new brain metastasis. This is the first time that meclofenamate will be used in patients with brain metastasis. This is a pilot study which means that the purpose of this study is to determine if a larger clinical trial of meclofenamate is possible in patients with brain metastasis. This study also aims to find out what effects, good and/or bad meclofenamate has on the patient and the cancer that has spread to the brain. The investigators also want to learn more about potential effects that this drug may have in the digestive system.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 18 Years - 80 Years
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

  • - Age 18-80.
  • - KPS ≥ 60.
  • - At least one recurrent or progressive brain metastasis (es) from any solid primary tumor that is visible on MRI as assessed by the patient's treating physician.
  • - Recurrence may occur after any treatment: recurrence after whole-brain radiation, stereotactic radiosurgery, surgical resection, systemic chemotherapy are all acceptable.
  • - There is no limit on the number of brain metastases.
  • - Surgical resection or SRS to other recurrent lesions in the same patient are acceptable, provided one recurrent lesion remains untreated.
  • - Systemic disease must be well-controlled or NED in the opinion of the patient's primary oncologist.

Exclusion Criteria:

  • - Inability to get brain MRI +/- contrast.
  • - Progressive systemic disease.
  • - Known leptomeningeal metastases.
  • - Primary Brain tumor.
  • - Active Intracranial Hemorrhage.
  • - Surgery less than two weeks before enrollment.
  • - GI hemorrhage (active or in recent 6 months) - Concurrent anti-platelet therapy.
  • - Concurrent anti-coagulation therapy.
  • - Active bleeding diathesis.
  • - Platelet count ≤ 70,000/mm3.
  • - International normalized ratio (INR) > 1.6 and a Partial Thromboplastin Time (PTT) > 40 seconds.
  • - Serum Creatinine >2 mg/dL OR CrCL <30ml/min.
  • - AST or ALT > 200 U/L.
  • - Hemoglobin <8 g/dL.
  • - Allergy to meclofenamate or other NSAID.
  • - Inability to tolerate PO dosing.
  • - Steroid dose increased in the most recent two weeks.
  • - Pregnancy.
  • - Cardiac Arrhythmia requiring medical management and/or pacemaker.
- Known congestive heart failure requiring medical management

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT02429570
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

N/A
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Memorial Sloan Kettering Cancer Center
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

Adrienne Boire, MD, PhD
Principal Investigator Affiliation Memorial Sloan Kettering Cance Center
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other
Overall Status Active, not recruiting
Countries United States
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Recurrent Brain Metastases, Progressive Brain Metastases
Study Website: View Trial Website
Arms & Interventions

Arms

Experimental: Meclofenamate

All enrolled patients will receive the study drug, meclofenamate at 100 mg PO BID.

Interventions

Drug: - Meclofenamate

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

Baptist Health South Florida, Miami, Florida

Status

Address

Baptist Health South Florida

Miami, Florida, 33143

Memorial Sloan Kettering Cancer Center, Basking Ridge, New Jersey

Status

Address

Memorial Sloan Kettering Cancer Center

Basking Ridge, New Jersey,

Memorial Sloan Kettering Monmouth, Middletown, New Jersey

Status

Address

Memorial Sloan Kettering Monmouth

Middletown, New Jersey, 07748

Commack, New York

Status

Address

Memorial Sloan Kettering Cancer Center at Commack

Commack, New York, 11725

Memorial Sloan Kettering Westchester, Harrison, New York

Status

Address

Memorial Sloan Kettering Westchester

Harrison, New York, 10604

Memorial Sloan Kettering Cancer Center, New York, New York

Status

Address

Memorial Sloan Kettering Cancer Center

New York, New York, 10065

Lehigh Valley Health Network, Allentown, Pennsylvania

Status

Address

Lehigh Valley Health Network

Allentown, Pennsylvania, 18103

Resources

  • Patient and Caregiver Survey
  • Clinical Trial Endpoints
  • Research Resources
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The content provided on clinical trials is for informational purposes only and is not a substitute for medical consultation with your healthcare provider. We do not recommend or endorse any specific study and you are advised to discuss the information shown with your healthcare provider. While we believe the information presented on this website to be accurate at the time of writing, we do not guarantee that its contents are correct, complete, or applicable to any particular individual situation. We strongly encourage individuals to seek out appropriate medical advice and treatment from their physicians. We cannot guarantee the availability of any clinical trial listed and will not be responsible if you are considered ineligible to participate in a given clinical trial. We are also not liable for any injury arising as a result of participation.

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