Journal of Vaccines & Clinical Trials

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Special Issue Article, Jvct Vol: 4 Issue: 3

Ethical challenges in pediatric neurology clinical trials

Abstract
During the last decade, number of clinical trials have been offered to pediatric patients with neurological disorders.

 

Dravet syndrome (DS) or severe myoclonic epilepsy in infancy is one of the most well-known disorders of the epileptic encephalopathies. DS is a highly treatment-resistant and refractory epilepsy syndrome. Establishment of a seizure free condition in affected children, even with anticonvulsant drug polypharmacy, is extremely rare.

 

Duchenne muscular dystrophy (DMD) is a disabling and life-threatening X-linked genetic disorder affecting males. Boys with DMD develop progressive proximal muscle weakness that leads to deterioration of ambulation, wheelchair dependency, and eventual respiratory and cardiac failure.

 

Spinal Muscular Atrophy (SMA) is an autosomal recessive neuromuscular disease resulting in atrophy of the voluntary muscles of the limbs and trunk. It is the most common genetic cause of infant mortality, and a major cause of childhood morbidity in the U.S.

 

Clinical trials in pediatric neurology rare diseases are testing new investigational drugs (IDs). There is still an ethical dilemma if the new treatment will be better than the standard of care. There are number of unknown risks. Patient’s enrollment can be very challenging. The commitment from the families is huge. Most of the clinical trials start with the double-blind, placebo controlled design. Families have to agree on the possibility for their child to be randomized in the placebo arm. Those clinical trials might have very frequent study visits which might cause financial burden. Lot of work needs to be done to address the ethical challenges.

 

 

Description: C:\Users\Dell\Desktop\Valued Abstracts\BC Children Vesna.png

                                                            Description: C:\Users\Dell\Desktop\Valued Abstracts\1 Asterey.jpg

 

 

 

Biography:

Vesna Popovska has graduated from medical school in 1988, and completed her residency in Ob/Gyn in 1998 in Skopje, Macedonia.  She moved to Canada in 1999 and joined the Division of Maternal Fetal Medicine at BC Women’s Hospital, where she established and lead the MFM Research Program.  In 2005, she was recruited by the Neurosciences Program at BC Children’s Hospital, as a senior research manager. She developed and led the program, becoming its director in 2016.  She is involved in the strategic planning, and develops collaborative relationship among universities, industry partners and CROs to support and advance patient-oriented research.

 

Speaker Publications:

 

  1. “Levels of antibodies against cytomegalovirus and Chlamydophila pneumoniae are increased in early onset pre-eclampsia”;International Journal of Obstetrics & Gynaecology / 2003 / 110(8):725-30
  2. “Grasrots and inhibitors on radicalization in north macedonia: Towards a systematic approach”; Law and politics / 2019 / 10.22190/FULP1902173P
  3. “The Urge for Comprehensive Cyber Security Strategies in the Western Balkan”; Information & Security: An International Journal / 2016 / Volume 34, Issue 1, p.25-36

 

10th International Conference on Clinical Research and Clinical Trials; Amsterdam, Netherlands- March 18-19, 2020.

 

Abstract Citation:

Ethical challenges in pediatric neurology clinical trials                                        ,Euro Clinical Trials 2020, 10th International Conference on Clinical Research and Clinical Trials; Amsterdam, Netherlands- March 18-19, 2020 (https://clinicaltrials.pharmaceuticalconferences.com/abstract/2020/ethical-challenges-in-pediatric-neurology-clinical-trials)

Abstract

Abstract
During the last decade, number of clinical trials have been offered to pediatric patients with neurological disorders.

 

Dravet syndrome (DS) or severe myoclonic epilepsy in infancy is one of the most well-known disorders of the epileptic encephalopathies. DS is a highly treatment-resistant and refractory epilepsy syndrome. Establishment of a seizure free condition in affected children, even with anticonvulsant drug polypharmacy, is extremely rare.

 

Duchenne muscular dystrophy (DMD) is a disabling and life-threatening X-linked genetic disorder affecting males. Boys with DMD develop progressive proximal muscle weakness that leads to deterioration of ambulation, wheelchair dependency, and eventual respiratory and cardiac failure.

 

Spinal Muscular Atrophy (SMA) is an autosomal recessive neuromuscular disease resulting in atrophy of the voluntary muscles of the limbs and trunk. It is the most common genetic cause of infant mortality, and a major cause of childhood morbidity in the U.S.

 

Clinical trials in pediatric neurology rare diseases are testing new investigational drugs (IDs). There is still an ethical dilemma if the new treatment will be better than the standard of care. There are number of unknown risks. Patient’s enrollment can be very challenging. The commitment from the families is huge. Most of the clinical trials start with the double-blind, placebo controlled design. Families have to agree on the possibility for their child to be randomized in the placebo arm. Those clinical trials might have very frequent study visits which might cause financial burden. Lot of work needs to be done to address the ethical challenges.

 

 

Description: C:\Users\Dell\Desktop\Valued Abstracts\BC Children Vesna.png

                                                            Description: C:\Users\Dell\Desktop\Valued Abstracts\1 Asterey.jpg

 

 

 

Biography:

Vesna Popovska has graduated from medical school in 1988, and completed her residency in Ob/Gyn in 1998 in Skopje, Macedonia.  She moved to Canada in 1999 and joined the Division of Maternal Fetal Medicine at BC Women’s Hospital, where she established and lead the MFM Research Program.  In 2005, she was recruited by the Neurosciences Program at BC Children’s Hospital, as a senior research manager. She developed and led the program, becoming its director in 2016.  She is involved in the strategic planning, and develops collaborative relationship among universities, industry partners and CROs to support and advance patient-oriented research.

 

Speaker Publications:

 

  1. “Levels of antibodies against cytomegalovirus and Chlamydophila pneumoniae are increased in early onset pre-eclampsia”;International Journal of Obstetrics & Gynaecology / 2003 / 110(8):725-30
  2. “Grasrots and inhibitors on radicalization in north macedonia: Towards a systematic approach”; Law and politics / 2019 / 10.22190/FULP1902173P
  3. “The Urge for Comprehensive Cyber Security Strategies in the Western Balkan”; Information & Security: An International Journal / 2016 / Volume 34, Issue 1, p.25-36

 

10th International Conference on Clinical Research and Clinical Trials; Amsterdam, Netherlands- March 18-19, 2020.

 

Abstract Citation:

Ethical challenges in pediatric neurology clinical trials                                        ,Euro Clinical Trials 2020, 10th International Conference on Clinical Research and Clinical Trials; Amsterdam, Netherlands- March 18-19, 2020 (https://clinicaltrials.pharmaceuticalconferences.com/abstract/2020/ethical-challenges-in-pediatric-neurology-clinical-trials)

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