Owings Mills, Maryland Clinical Trials

A listing of Owings Mills, Maryland clinical trials actively recruiting patient volunteers.

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Found 181 clinical trials
A Dose Study of Doxil in a Dose Dense 14 Day CDOP/Rituximab Regimen for Patients With Diffuse Large B-Cell Non-Hodgkin Lymphoma (NHL)> 60 Years or With Compromised Cardiac Status.

The purpose of this study is to evaluate the feasibility and tolerability of delivering a full dose, on time schedule of dose-dense CDOP-R (cyclophosphamide, doxil, vincristine, prednisone, and rituximab) in NHL.

ejection fraction
diffuse large b-cell lymphoma
rituximab
vincristine
pegfilgrastim
Sinai Hospital of Baltimore
 (7.7 away) Contact site
  • 33 views
  • 07 Nov, 2020
  • 1 location
Timolol for the Treatment of Acne and Rosacea

This research is being done to determine the safety and tolerability of timolol in the treatment of acne and rosacea. The investigators will also look for specific biomolecular changes in acne or rosacea skin when it is exposed to timolol. Timolol is approved by the Food and Drug Administration (FDA) …

rosacea
erythema
acne
blackheads
flushing
Johns Hopkins Dermatology Department
 (6.7 away) Contact site
  • 1921 views
  • 01 Feb, 2021
  • 1 location
Palbociclib in Treating Patients With Relapsed or Refractory Rb Positive Advanced Solid Tumors Non-Hodgkin Lymphoma or Histiocytic Disorders With Activating Alterations in Cell Cycle Genes (A Pediatric MATCH Treatment Trial)

This phase II Pediatric MATCH trial studies how well palbociclib works in treating patients with Rb positive solid tumors, non-Hodgkin lymphoma, or histiocytic disorders with activating alterations (mutations) in cell cycle genes that have spread to other places in the body and have come back or do not respond to …

solid tumour
pegfilgrastim
solid tumor
autologous stem cell infusion
palbociclib
Sinai Hospital of Baltimore
 (7.7 away) Contact site
  • 115 views
  • 12 Sep, 2021
  • +80 other locations
A Study to Investigate the Efficacy Safety and Tolerability of JNJ-42165279 in Adolescent and Adult Participants With Autism Spectrum Disorder

The purpose of this study is to evaluate the efficacy of JNJ-42165279 compared with placebo in the improvement of symptoms of Autism Spectrum Disorder (ASD) during 12 weeks of treatment using the Autism Behavior Inventory (ABI).

psychiatric disorder
pervasive developmental disorder
autism
behavior modification
Sheppard Pratt Health System
 (9.3 away) Contact site
  • 550 views
  • 02 Jun, 2021
  • +12 other locations
Post Approval Study of the Eversense Continuous Glucose Monitoring

A Post Approval Study to Evaluate the Long-term Safety and Effectiveness of the Eversense Continuous Glucose Monitoring (CGM) System over repeat insertion and removal cycles and to demonstrate the long-term safety of the Eversense CGM System

continuous glucose monitoring
diabetes
MODEL Clinical research
 (7.6 away) Contact site
  • 506 views
  • 08 Aug, 2021
  • +16 other locations
MILD Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims Study

This prospective longitudinal study will compare incidence rates of Medicare beneficiary surgical and minimally invasive intervention post index procedure, as well as harms associated with the MILD procedure, at 24 months post-treatment with MILD, tested against a control group of similar patients that have had a comparable procedure. This study …

ClearWay Pain Solutions
 (0.5 away) Contact site
  • 13680 views
  • 16 Sep, 2021
  • +897 other locations
Screening Protocol for Tumor Antigen Expression Profiling and HLA Typing for Eligibility Determination

This screening study is intended for men and women at least 18 years of age who have advanced solid or hematologic malignancy. The study will assess a subject's human leukocyte antigen (HLA) subtype and tumor antigen expression profile. Based on the results, it will be determined if a subject is …

UM St. Joseph Medical Center
 (9.3 away) Contact site
  • 0 views
  • 22 Mar, 2021
  • +27 other locations
A Registry for Participants With Chronic Hypoparathyroidism

This is a prospective, observational disease and drug registry designed to evaluate the safety and effectiveness profile of rhPTH(1-84) under conditions of routine clinical practice and to observe the clinical course of chronic hypoparathyrodism. No treatment is provided as a result of participating in this registry and all decisions on …

Model Clinical Research
 (9.3 away) Contact site
  • 789 views
  • 19 Mar, 2021
  • +144 other locations
The RECOVER sUb-study Which Leverages quaNtitative and Credible Research tOols From Verily Will providE Assessment measuRes for Depressive Episodes

The objective of this study is to collect both active and passive data using a wearable, multi-sensor device (Verily Study Watch) and phone application (Mood App) which aims to capture mental health status, in subjects participating in the RECOVER clinical trial (A Prospective, Multi-center, Randomized Controlled Blinded Trial Demonstrating the …

Aaronson
 (7.6 away) Contact site
  • 0 views
  • 22 Aug, 2021
  • +19 other locations
Time and Motion Study for Ocrelizumab and Ofatumumab Administration in Relapsing Multiple Sclerosis

This is an observational cross-sectional study of Ocrelizumab or Ofatumumab administrations for Relapsing forms of Multiple Sclerosis (RMS) in selected sites in the US, the UK and Australia.

Novartis Investigative Site
 (6.5 away) Contact site
  • 0 views
  • 13 Jun, 2021
  • +12 other locations