In Utero Enzyme Replacement Therapy for Lysosomal Storage Diseases

Wolman Disease Clinical Trial

— IUERT  

Official title:

In Utero Enzyme Replacement Therapy (ERT) for Prenatally Diagnosed Lysosomal Storage Disorders (LSDs).

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04532047
• Other study ID #: 20-31520
• Status: Recruiting
• Phase: Phase 1
• Start date: July 1, 2021
• Est. completion date: July 2032

Study information

• Verified date: September 2023
• Source: University of California, San Francisco
• Contact: Tippi MacKenzie, MD
• Phone: 415-476-4086
• Email: tippi.mackenzie[@]ucsf.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators aims to determine the the maternal and fetal safety and feasibility of in utero fetal enzyme replacement therapy in fetuses with Lysosomal Storage Diseases.

Description:

Because fetuses with these LSDs are at increased risk of serious perinatal morbidity and mortality, particularly in the setting of Non-Immune Hydrops Fetalis (NIHF), the administration of the approved enzyme therapy in utero has the potential to significantly improve outcomes for affected fetuses. The perinatal death rate associated with NIHF ranges from 30 to 75%, so development of an in utero approach to treatment could be of significant benefit. The in utero period has been shown to be a time of relative fetal tolerance to immune stimuli, and this tolerance may lead to improved response to ERT in situations where postnatal initiation instead leads to antibody development and impaired response to treatment. It is also probable that in some cases, initiation of ERT in utero leads to improved neurodevelopmental outcomes if the replaced enzyme impacts the neurologic system during critical periods of development. This is a phase 1 clinical trial to determine the safety and feasibility of fetal enzyme replacement therapy in fetuses with LSD

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 10
• Est. completion date: July 2032
• Est. primary completion date: July 2031
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Live male or female fetuses at 18 0/7 weeks to 34 6/7 weeks gestation
• Diagnosis of one of the 8 included LSDs in utero by genetic or enzymatic analyses performed on amniotic fluid, fetal blood, placental tissue, or other samples through chorionic villus sampling (CVS), amniocentesis, cordocentesis, cell free fetal DNA, or other procedures. In the event that parents are identified as genetic carriers for a LSD, diagnostic testing for the fetus would be performed to confirm the diagnosis
• Pregnant women age 18 years to 50 years, carrying a live male or female fetus at 18 0/7 weeks to 34 6/7 weeks gestation
• Identified through the above listed means to be carrying a fetus with an LSD.
• Ability to give written informed consent and comply with the requirements of the study.

Exclusion Criteria:

• Fetuses with a concurrent severe structural anomaly
• Fetuses with an additional pathogenic genetic variant not related to the underlying LSD that contribute a significant risk of morbidity or mortality. Hydrops fetalis will not be an exclusion criterion because ERT has the possibility of significant benefit in this situation.
• Women with one or more significant comorbidities that would preclude fetal

intervention including, but not limited to:

1. inability to complete the procedure secondary to maternal body habitus or placental location

2. significant cardiopulmonary disease

3. mirror syndrome

4. end organ failure

5. altered mental status

6. placental abruption

7. active preterm labor

8. preterm premature rupture of membranes.

• Mother will require therapeutic dosing of anticoagulation within 24 hours prior to or following the intervention.

Related Conditions & MeSH terms

• Gaucher Disease
• Gaucher Disease, Type 2
• Gaucher Disease, Type 3
• Glycogen Storage Disease Type II
• MPS I
• MPS II
• MPS IVA
• MPS VI
• Mps VII
• Pompe Disease Infantile-Onset
• Wolman Disease

Intervention

Drug:
• Aldurazyme (laronidase)
Enzyme replacement therapy for lysosomal storage diseases

Locations

Country	Name	City	State
United States	University of California	San Francisco	California

Sponsors (2)

Lead Sponsor	Collaborator
University of California, San Francisco	Duke University

Country where clinical trial is conducted

United States, 

References & Publications (9)

Azevedo AC, Schwartz IV, Kalakun L, Brustolin S, Burin MG, Beheregaray AP, Leistner S, Giugliani C, Rosa M, Barrios P, Marinho D, Esteves P, Valadares E, Boy R, Horovitz D, Mabe P, da Silva LC, de Souza IC, Ribeiro M, Martins AM, Palhares D, Kim CA, Giugl — View Citation

Banugaria SG, Prater SN, Ng YK, Kobori JA, Finkel RS, Ladda RL, Chen YT, Rosenberg AS, Kishnani PS. The impact of antibodies on clinical outcomes in diseases treated with therapeutic protein: lessons learned from infantile Pompe disease. Genet Med. 2011 A — View Citation

Blitz MJ, Rochelson B, Sood M, Bialer MG, Vohra N. Prenatal sonographic findings in a case of Wolman's disease. J Clin Ultrasound. 2018 Jan;46(1):66-68. doi: 10.1002/jcu.22481. Epub 2017 Apr 4. — View Citation

Chien YH, Lee NC, Thurberg BL, Chiang SC, Zhang XK, Keutzer J, Huang AC, Wu MH, Huang PH, Tsai FJ, Chen YT, Hwu WL. Pompe disease in infants: improving the prognosis by newborn screening and early treatment. Pediatrics. 2009 Dec;124(6):e1116-25. doi: 10.1 — View Citation

Meikle PJ, Hopwood JJ, Clague AE, Carey WF. Prevalence of lysosomal storage disorders. JAMA. 1999 Jan 20;281(3):249-54. doi: 10.1001/jama.281.3.249. — View Citation

Nguyen QH, Witt RG, Wang B, Eikani C, Shea J, Smith LK, Boyle G, Cadaoas J, Sper R, MacKenzie JD, Villeda S, MacKenzie TC. Tolerance induction and microglial engraftment after fetal therapy without conditioning in mice with Mucopolysaccharidosis type VII. — View Citation

Platt FM, d'Azzo A, Davidson BL, Neufeld EF, Tifft CJ. Author Correction: Lysosomal storage diseases. Nat Rev Dis Primers. 2018 Oct 18;4(1):36. doi: 10.1038/s41572-018-0037-0. — View Citation

Rosenbloom BE, Weinreb NJ. Gaucher disease: a comprehensive review. Crit Rev Oncog. 2013;18(3):163-75. doi: 10.1615/critrevoncog.2013006060. — View Citation

Tsai AC, Hung YW, Harding C, Koeller DM, Wang J, Wong LC. Next generation deep sequencing corrects diagnostic pitfalls of traditional molecular approach in a patient with prenatal onset of Pompe disease. Am J Med Genet A. 2017 Sep;173(9):2500-2504. doi: 1 — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Number of participants that show functional cardiac, growth, mobility, and neurocognitive function.	ecogardiogram, skeletal survey, neurocognitve assessments such as Bayley III to assess cardiac, growth, mobility and neurocognitive function.	6 years
Primary	Number of participants with treatment-related adverse events as assessed by CTCAE v5.0.	Adverse and serious adverse events including, but not limited to, death within 24 hours after the procedure, stillbirth, death prior to initial hospital discharge,increased response with antibody development above that expected with postnatal ERT, and serious related or serious unexpected adverse events exceeding those expected with the natural history of treated disease during the first five years of life, assessed by CTCAE v5.0.	6 years
Primary	Number of participants to receive the full initial, weight-based dose of enzyme replacement therapy through the fetal umbilical vein, and subsequent doses throughout the pregnancy.	full dose administration compared to the need to halt the intervention prior to administration of a full dose.	6 years
Primary	Number of participants with the presence and levels of glycosaminoglycans (GAGs) in urine.	Laboratory analysis of urine for GAG levels.	6 years
Primary	The number of participants with improvement or resolution of hydrops (if present).	Improvement of hydrops via ultrasound and echocardiogram results (if present).	6 years
Secondary	Number of participants that show measured levels of antibodies against the enzyme.	Laboratory analysis of blood to measure antibody levels.	6 years