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Methotrexate Medical Research Studies

Up-to-date List of Methotrexate Medical Research Studies

What Research is Being Done?

A clinical study involves research using human volunteers (also called participants) that is intended to add to medical knowledge. There are two main types of clinical studies: clinical trials (also called interventional studies) and observational studies. Following list includes both interventional and observational studies.

Latest Methotrexate Medical Research Studies

Rank Status Study
1 Recruiting Individualized High Dose Methotrexate to Treat Cancer in Children Who Have a Significant Risk for Side Effects to Methotrexate
Condition: Cancer
Intervention: Drug: Methotrexate
Outcome Measures: Incidence of success (achieving an end infusion peripheral blood Methotrexate concentration between 50-80 μM);   Incidence of nephrotoxicity;   Incidence of neurotoxicity;   Incidence of mucositis;   Incidence of hepatoxicity;   Incidence of myelosuppression
2 Unknown  Methotrexate and Temozolomide Versus Methotrexate, Procarbazine, Vincristine and Cytarabine
Condition: Lymphoma
Interventions: Drug: Methotrexate and temozolomide;   Drug: Methotrexate , procarbazine ,vincristine ,cytarabine
Outcome Measures: Progression-free survival;   Overall survival:median and overall survival;   Response rates;   Toxicity;   Late toxicity
3 Not yet recruiting The Efficiency Of The Methotrexate At Patients Affected By Grave Pelade
Condition: ALOPECIA AREATA
Intervention: Drug: Methotrexate
Outcome Measures: OUTCOME MESURE;   SECONDARY OUTCOME MEASURE
4 Recruiting A Phase 2b/3 Study to Evaluate Efficacy and Safety of Masitinib in Comparison to Methotrexate in Patients With Active Rheumatoid Arthritis With Inadequate Response to Methotrexate or to Any Disease-Modifying Antirheumatic Drug
Condition: Rheumatoid Arthritis (RA)
Interventions: Drug: masitinib;   Drug: Methotrexate
Outcome Measures: ACR50;   ACR
5 Not yet recruiting The Effects of Methotrexate Therapy on ST Segment Elevation MYocardial InfarctionS (TETHYS Trial)
Condition: Myocardial Infarction
Interventions: Drug: Methotrexate;   Drug: Riboflavin
Outcome Measures: Area under the curve of creatine kinase;   Area under the curve for creatine kinase MB fraction and troponin I high sensitive;   Compare the peaks of CK, CK-MB and troponin I ultra-sensitive;   Compare the levels of high-sensitivity C-reactive protein at admission, after 72 hours and after 3 months;   Compare the levels of erythrocyte sedimentation rate on admission and after 72 hours;   Compare B-type natriuretic peptide (BNP) levels on admission, after 72 hours and after 3 months;   Compare the "TIMI frame count" of the culprit artery;   Compare the Killip score on admission and after 72 hours;   Assess ventricular ejection fraction with transthoracic echocardiography during the first 72 hours after 3 months;   Assess mortality at 3 months;   Evaluate reinfarction in 3 months;   Rate side effects
6 Not yet recruiting VACcination In Methotrexate Treated Rheumatoid Arthritis Patients
Condition: Rheumatoid Arthritis
Interventions: Biological: Prevenar 13;   Biological: Pneumo23;   Drug: Methotrexate
Outcome Measures: rate of immunological positive answer 1 month after antipneumococcal vaccination by the conjugated vaccine Prevenar13 ® in patients suffering from rheumatoid polyarthritis.;   Number of patients in each group who will know fully immunological answer to 5 interest serotypes after the first antipneumococcal vaccination (Prevenar13);   Number of patients in each group who will know an immunological answer to 13 serotypes after the first antipneumococcal vaccination (Prevenar13);   Number of patients who will know a fully immunological answer (13 serotypes of vaccine) after a antipneumococcal revaccination with Pneumo 23.;   Number of patients who will suffer from adverse events in relation with the antipneumococcal vaccination;   Frequency of occurence of disease spurts from the first vaccination until the end of the study;   occurence of the pneumococcal disease from the first vaccination to the end of the study.
7 Recruiting Will the Use of Glucarpidase After Methotrexate Treatment Allow More Patients With Bone Sarcoma to Have Fewer Side Effects and Receive Subsequent Chemotherapy on Time?
Conditions: Osteosarcoma;   Spindle Cell Sarcoma of Bone
Interventions: Drug: Glucarpidase;   Drug: Methotrexate;   Drug: Folinic Acid
Outcome Measures: Estimate of the difference in proportions of patients ready to receive chemotherapy on Day 15 of each chemotherapy cycle comparing standard rescue and glucarpidase+standard rescue;   To investigate whether glucarpidase rescue after high-dose Methotrexate reduces the incidence of Methotrexate associated adverse effects;   Plasma Methotrexate concentration;   Incidence of glucarpidase related adverse effects;   Number of days required in hospital per cycle;   Assessment of quality of life;   Serum anti-glucarpidase IgG levels following glucarpidase administration;   To investigate whether glucarpidase rescue after high-dose Methotrexate reduces the severity of Methotrexate associated adverse effects;   To investigate whether glucarpidase rescue after high-dose Methotrexate reduces the duration of Methotrexate associated adverse effects;   Plasma DAMPA concentration;   Total dose of folinic acid rescue required per cycle
8 Not yet recruiting Methotrexate for Central Serous Chorioretinopathy Treatment Trial
Condition: Central Serous Chorioretinopathy
Interventions: Drug: Methotrexate;   Drug: Delayed treatment
Outcome Measure: Optical Coherence Tomography indicating the level of central serous detachment
9 Recruiting Tac, Mini-MTX, MMF Versus Tac, MTX for GVHD Prevention
Conditions: Chronic Myelogenous Leukemia;   Acute Lymphoblastic Leukemia;   Acute Myeloid Leukemia;   Acute Biphenotypic Leukemia;   Myelodysplastic Syndrome;   Myeloproliferative Neoplasm;   Non-Hodgkin Lymphoma;   Hodgkins Disease;   Chronic Lymphocytic Leukemia;   Multiple Myeloma
Interventions: Drug: tacrolimus;   Drug: Methotrexate;   Drug: Mycophenolate mofetil;   Drug: Methotrexate (low dose)
Outcome Measures: Incidence of severe (grade 3-4) mucositis graded according to the World Health Organization (WHO) grading scale;   Time to neutrophil engraftment;   Time to platelet engraftment;   Incidence of acute GVHD;   Length of hospitalization;   Use of total parenteral nutrition (TPN);   Overall survival defined by Center for International Blood and Marrow Transplant Research (CIBMTR) criteria for individual diseases;   Progression-free survival defined by CIBMTR criteria for individual diseases;   Incidence of chronic GVHD;   Length of time on continuous infusion narcotics;   Incidence of infection;   Incidence of hepatotoxicity;   Incidence of nephrotoxicity;   Incidence of pulmonary toxicity
10 Recruiting Tacrolimus/Methotrexate Versus Cyclosporine/Methotrexate for Prophylaxis of Graft Versus Host Disease
Condition: Graft vs Host Disease
Interventions: Drug: Tacrolimus;   Drug: Cyclosporine;   Drug: Methotrexate
Outcome Measures: incidence of grade II-IV acute graft versus host disease;   incidence of infection;   incidence of adverse drug reactions
11 Recruiting Methotrexate Treatment for Ectopic Pregnancy
Condition: Ectopic Pregnancy
Interventions: Procedure: Single-dose Methotrexate;   Procedure: Two-dose Methotrexate protocol
Outcome Measure: treatment success
12 Recruiting Initial Treatment With Golimumab in Early PsA
Condition: Psoriatic Arthritis
Interventions: Drug: golimumab;   Drug: Methotrexate
Outcome Measures: Percentage of patients achieving DAS remission response criteria;   Number of Participants with Adverse Events;   Number of patients fulfilling Minimal Disease activity criteria and other outcome measurements
13 Recruiting Methotrexate or Dactinomycin in Treating Patients With Low-Risk Gestational Trophoblastic Neoplasia
Conditions: Gestational Trophoblastic Tumor;   Hydatidiform Mole;   Low Risk Metastatic Gestational Trophoblastic Tumor;   Uterine Choriocarcinoma
Interventions: Drug: leucovorin calcium;   Biological: dactinomycin;   Drug: Methotrexate;   Procedure: quality-of-life assessment
Outcome Measures: Complete response vs treatment failure;   Severity of adverse events as assessed by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events version 4;   Overall QOL
14 Recruiting A Phase III Study to Evaluate the Efficacy and Safety of ENIA11 in Combination With Methotrexate Versus Methotrexate Alone in Patients With RA
Condition: Rheumatoid Arthritis
Interventions: Drug: Methotrexate;   Drug: ENIA11;   Drug: Placebo
Outcome Measure: ACR20 responder at last treatment visit
15 Recruiting Prospective, Multicentric, Phase II Randomized Controlled Trial on Two Parallel Groups Comparing the Efficacy of Two Immunosuppressive Drugs (Methotrexate, Cyclophosphamide) in Large Granular Lymphocytes Leukemia
Condition: Large Granular Lymphocytes Leukemia
Interventions: Drug: Methotrexate;   Drug: Cyclophosphamide
Outcome Measures: Complete response (CR);   overall response rate (ORR);   Hematological partial response (PR);   Progressive disease;   Time-to-relapse;   Molecular remission;   Adverse events rate;   Compliance;   relationship between the response to treatment and the phenotypic subtype
16 Recruiting Leflunomide Versus Sulfasalazine/Methotrexate in Rheumatoid Arthritis:an Ultrasound/Magnetic Resonance Imaging Study
Condition: Rheumatoid Arthritis
Interventions: Drug: Methotrexate plus sulfasalazine;   Drug: Leflunomide
Outcome Measures: MRI synovitis score;   MRI bone marrow edema score;   MRI erosion score;   US synovitis score;   clinical outcomes
17 Recruiting A Study on the Impact of Methotrexate Discontinuation on the Efficacy of Subcutaneous RoActemra/Actemra (Tocilizumab) With Methotrexate in Patients With Moderate to Severe Active Rheumatoid Arthritis
Condition: Rheumatoid Arthritis
Interventions: Drug: tocilizumab [RoActemra/Actemra];   Drug: Methotrexate;   Drug: placebo
Outcome Measures: Change in disease activity (DAS28) scores;   Change in bone erosion scores for patients in the MRI substudy;   Percentage of patients with a >/= 1.2 worsening in DAS28 between Week 24 and Weeks 40 and 52;   Percentage of patients achieving DAS 28 <2.6 and DAS28 </= 3.2 at Weeks 40 and 52;   Percentage of patients achieving ACR20/50/70 responses at Weeks 40 and 52;   Safety: Incidence of adverse events
18 Recruiting Methotrexate in the Treatment of Chronic Idiopathic Urticaria
Condition: Chronic Urticaria
Interventions: Drug: Methotrexate (Novatrex ®) + anti-H1;   Drug: Placebo + anti-H1
Outcome Measures: Number of patients with complete remission of urticaria at 18 weeks;   Tolerance : clinical and biological safety;   Efficacy of the treatment in improving symptoms : pruritus;   Persistency of the complete remission at 26 weeks;   Efficacy of the treatment in improving symptoms : outbreaks by week;   Efficacy of the treatment in improving symptoms : duration of lesions;   Efficacy of the treatment in improving quality of life;   Efficacy of the treatment in improving quality of sleep;   Efficacy of the treatment in improving facial/cervical urticarial lesions
19 Recruiting High-dose Methotrexate and Liposomal Cytarabine in Treating Patients With CNS Metastases From Breast Cancer
Conditions: Central Nervous System Metastases;   Leptomeningeal Metastases;   Recurrent Breast Cancer;   Stage IV Breast Cancer;   Tumors Metastatic to Brain
Interventions: Drug: Methotrexate;   Drug: liposomal cytarabine;   Other: quality-of-life assessment;   Other: questionnaire administration
Outcome Measures: Progression-free survival (PFS);   Cancer Therapy Evaluation Program (CTEP) Common Toxicity Criteria grade 3+ neurological and systemic toxicity that persists following dose reductions or schedule modifications;   Overall survival;   Duration of response;   Cytologic response as measured by CSF cytology (positive or negative for malignant cells);   FACT-Brain (Br) total score and subscales (physical well-being, social/family well-being, emotional well-being, functional well-being, symptom index) using standard scoring
20 Not yet recruiting Low-dose Methotrexate for Reduction GINA 5 Medications in Chronic Severe Asthma
Condition: Low Dose Methotrexate in Severe Chronic Asthma
Interventions: Drug: Methotrexate;   Drug: Placebo
Outcome Measures: At least 50% reduction in total dosage of GINA step 5 medications;   clinically significant changes in clinimetric scores

These studies may lead to new treatments and are adding insight into Methotrexate etiology and treatment.

A major focus of Methotrexate research is the development of new drugs and other treatment options. Studies seek to identify new drugs to treat various related disorders and to find safer, more effective doses for medications already being used. Other research is aimed at identifying receptors or drug targets.


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