This study will examine post-natal neurologic and cognitive development of infants who may have been exposed to tanezumab or comparator in-utero during the tanezumab clinical program (whether the exposure is through maternal or paternal participation in a tanezumab clinical study).
This study will enroll infants with potential tanezumab exposure in utero at sites overseen by Schulman and Associates IRB This study will attempt to enroll all infants who qualify.
Study Type
OBSERVATIONAL
Enrollment
7
This study will examine post-natal neurologic and cognitive development of infants who may have been exposed to tanezumab or comparator in-utero during the tanezumab clinical program (whether the exposure is through maternal or paternal participation in a tanezumab clinical study).
Pfizer Investigational Site
Tempe, Arizona, United States
Pfizer Investigational Site
Tempe, Arizona, United States
Pfizer Investigational Site
Wildomar, California, United States
Pfizer Investigational Site
Cutler Bay, Florida, United States
Bayley Infant Neurodevelopmental Screener
Time frame: 0-2 Months
Bayley Infant Neurodevelopmental Screener
Time frame: 8 months
Bayley Infant Neurodevelopmental Screener
Time frame: 15 months
Receptive-Expressive Emergent Language Test
Time frame: 0-2 Months
Receptive-Expressive Emergent Language Test
Time frame: 8 months
Receptive-Expressive Emergent Language Test
Time frame: 15 months
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Pfizer Investigational Site
Duncansville, Pennsylvania, United States
Pfizer Investigational Site
Memphis, Tennessee, United States
Pfizer Investigational Site
Houston, Texas, United States
Pfizer Investigational Site
Salt Lake City, Utah, United States