Sponsor or institution
Clinical trials and research at Phoenix Nest, INC.
As of November 12, 2026, Find a Trial lists 6 NIH-funded research projects at this institution, with $5.8 million in listed awards. Every study is explained in plain English. Data from ClinicalTrials.gov and NIH RePORTER, updated November 12, 2026.
- 6NIH research projects
NIH-funded research (6)
Early-stage science funded by the US National Institutes of Health. Most of these projects don't enroll patients, but they show what is being worked on.
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Gene therapy manufacturing and testing for a rare brain disease (MPS IIIC) to help affected children
A NIH-funded project aims to develop and refine the manufacturing and analytical processes for a gene therapy intended to help children with MPS IIIC, a rare and progressive neurological disease.
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Biomarkers and clinical tools for Sanfilippo syndrome type C (MPS IIIC)
Create new lab tests and clinical tools to help detect and follow MPS IIIC (Sanfilippo type C) in affected children and adults.
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Finding new biomarkers and tools for Mucopolysaccharidosis IIIC patients.
This study is looking for ways to better diagnose and manage Mucopolysaccharidosis Type IIIC, a rare condition, by finding helpful markers in the body and improving how we track the disease, so patients can get better care and support.
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Investigating treatments for a rare childhood brain disorder called MPS IIID.
This study is looking at a new treatment for Mucopolysaccharidosis IIID, a rare condition that affects how children's brains develop, and it aims to help improve their quality of life by delivering a special enzyme directly into the brain.
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Investigating a new treatment for a rare childhood neurodegenerative disorder.
This study is testing a new treatment that delivers a special enzyme directly into the brain to help children with Mucopolysaccharidosis IIID, a rare condition that affects their development and thinking skills, with the hope of improving their health and quality of life.
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Creating a gene therapy for Sanfilippo Syndrome Type C
This study is testing a new gene therapy for people with Sanfilippo Syndrome Type C, a rare condition that affects the brain, to see if it can help by fixing the genetic problem that causes the disease and improve their quality of life.
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