The largest CBD study
presented efficacy and safety data on GW Pharmaceutical's investigational medicine, Epidiolex (cannabidiol) from open - label Expanded Access programs at 16 sites.
Not exact matches
Three studies
presented at the American Epilepsy Society's 69th Annual Meeting in Philadelphia highlight emerging
efficacy and safety data of Epidiolex, a pharmaceutical liquid formulation of cannabidiol, which is currently undergoing U.S. Food
and Drug Administration (FDA) authorized Phase 3 pivotal clinical trials in the United States
and across the globe by GW Pharmaceuticals.
Rwanda will
present safety and efficacy data on 50 patients at the American Urology Association in May 2011,
and a randomized, controlled trial with 150 participants, designed to compare PrePex with the conventional surgical method is currently ongoing.
The documentation ranges across the whole spectrum of drug development: Investigators» brochures provide information on all that is currently known about the medicine
and so need periodic updating; accurate
and concise protocols are required to ensure that trials are performed effectively; clinical trial reports (generally from phase II
and III studies)
present the information gathered from the trials; higher level documents provide summaries of
efficacy and safety data from clinical trial programmes; expert reports provide critical interpretation of the results;
and response documents clarify any points that are not clear to the regulatory agencies or provide additional analyses or supporting data for any items of concern.
Early results from a phase I, first in - human study indicate that a potential new class of drugs, RNA interference (RNAi) drugs, can be safely administered in humans, according to a researcher who
presented data on the
safety and preliminary
efficacy of TKM - 080301 at the AACR Annual Meeting 2013, held in Washington, D.C., April 6 - 10.
At the International Society for Stem Cell Research 2017 Annual Meeting (June 14 - 17, 2017; Boston, USA), Asterias Biotherapeutics, Inc (CA, USA) will
present new 9 - month
efficacy and safety data from their ongoing SCiStar Phase I / IIa trial of human embryonic stem cell - derived oligodendrocyte progenitor cells.
Asterias Biotherapeutics, Inc will
present new 9 - month
efficacy and safety data from their ongoing Phase I / IIa trial for OPC - 1 in a workshop
and poster presentation.
AST - VAC1 (antigen -
presenting autologous dendritic cells) is an autologous cancer immunotherapy with promising
efficacy and safety data from a Phase 2 study in Acute Myeloid Leukemia (AML).
The drug was approved based on
efficacy and safety results from a phase III trial
presented earlier this year at the 2015 American Society of Clinical Oncology Annual Meeting.
It is at
present unknown whether an optimal balance between
safety and efficacy can be achieved with the combination therapy of GH
and IGF - I, since this combination has been evaluated in only a small number of patient populations
and in studies of a relatively short duration.
Charted
and recorded information in client files.Tracked client movement on
and off the unit by documenting times
and destinations of clients.Checked facility for open windows, locked doors, malfunctioning smoke detectors
and other
safety hazards.Quickly responded to crisis situations when severe mental health
and behavioral issues arose.Efficiently gathered information from families
and social services agencies to inform development of treatment plans.Documented all patient information including service plans, treatment reports
and progress notes.Collaborated closely with treatment team to appropriately coordinate client care services.Developed comprehensive treatment plans that focused on accurate diagnosis
and behavioral treatment of problems.Consulted with psychiatrists about client medication changes, issues with medicine compliance
and efficacy of medications.Organized treatment projects that focused on problem solving skills
and creative thinking.Referred clients to other programs
and community agencies to enhance treatment processes.Created
and reviewed master treatment
and discharge plans for each client.Guided clients in understanding illnesses
and treatment plans.Developed appropriate policies for the identification of medically - related social
and emotional needs of clients.Assisted clients in scheduling home visits
and phone calls
and monitored effectiveness of these activities.Evaluated patients for psychiatric services
and psychotropic medications.Monitored patients prescribed psychotropic medications to assess the medications» effectiveness
and side effects.Evaluated patients to determine potential need to transfer to specialized inpatient mental health facilities.Administered medication to patients
presenting serious risk of danger to themselves
and others.Conducted psychiatric evaluations
and executed medication management for both inpatient
and outpatient facilities.Led patients in individual, family, group
and marital therapy sessions.Diagnosed mental health, emotional
and substance abuse disorders.Recorded comprehensive patient histories
and coordinated treatment plans with multi-disciplinary team members.Consulted with
and developed appropriate treatment
and rehabilitation plans for dually diagnosed patients.Referenced
and used various therapy techniques, including psychodynamic, family systems, cognitive behavioral
and lifespan integration psychotherapy.