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1.
Ther Innov Regul Sci ; 56(6): 964-975, 2022 11.
Article in English | MEDLINE | ID: covidwho-1803265

ABSTRACT

The literature thoroughly describes the challenges of pediatric drug development for rare diseases. This includes (1) generating interest from sponsors, (2) small numbers of children affected by a particular disease, (3) difficulties with study design, (4) lack of definitive outcome measures and assessment tools, (5) the need for additional safeguards for children as a vulnerable population, and (6) logistical hurdles to completing trials, especially with the need for longer term follow-up to establish safety and efficacy. There has also been an increasing awareness of the need to engage patients and their families in drug development processes and to address inequities in access to pediatric clinical trials. The year 2020 ushered in yet another challenge-the COVID-19 pandemic. The pediatric drug development ecosystem continues to evolve to meet these challenges. This article will focus on several key factors including recent regulatory approaches and public health policies to facilitate pediatric rare disease drug development, emerging trends in product development (biologics, molecularly targeted therapies), innovations in trial design/endpoints and data collection, and current efforts to increase patient engagement and promote equity. Finally, lessons learned from COVID-19 about building adaptable pediatric rare disease drug development processes will be discussed.


Subject(s)
Biological Products , COVID-19 Drug Treatment , Child , Drug Development , Ecosystem , Humans , Pandemics , Public Health , Rare Diseases/drug therapy
2.
J Neurol ; 268(11): 3988-3991, 2021 Nov.
Article in English | MEDLINE | ID: covidwho-1163035

ABSTRACT

There have been considerations since the beginning of the Coronavirus pandemic that COVID-19 infection, like any other viral illness, can trigger neurological and metabolic decompensation in patients with mitochondrial diseases. At the time of writing, there were no published reports reviewing experiences and guidelines about management of COVID-19 infection in this patient population. We present a challenging case of an adult patient with a known diagnosis of Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like Episodes (MELAS) complicated by COVID-19 infection. She initially presented with altered mental status and vomiting and went on to develop a stroke-like episode, pancreatitis, and pneumatosis intestinalis. We review salient features of her hospitalization, including initiation of thromboprophylaxis in relation to intravenous arginine therapy, caution regarding medications such as remdesivir, and the incidence of gastrointestinal complications.


Subject(s)
Acidosis, Lactic , COVID-19 , MELAS Syndrome , Stroke , Venous Thromboembolism , Adult , Anticoagulants , Female , Humans , MELAS Syndrome/complications , MELAS Syndrome/therapy , SARS-CoV-2 , Stroke/complications
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