Overall UTMB plans to establish a nationally and internationally recognized center with the theme of Development of Medications and Biologics for Treatment of the Pregnant Patient and the Fetus. The overarching Center goal is to accelerate FDA approval of medications, biologics, and therapeutic modalities for treatment of the pregnant patient and/or her fetus. This goal will be achieved by 2 major objectives: (A) support, expand, and diversify the teams of investigators by recruitment, education, and training of junior faculty in the field of obstetric-fetal pharmacology and (B) augment the existing environment, tools, and infrastructure for clinical and translational projects. Our success is due, in part, to the clinical infrastructure present at UTMB, which includes access to a wide, diverse patient population via UTMB's Regional Maternal and Child Health Program as well as the cadre of trained research nurses in Ob/Gyn's Perinatal Research Division. Our translational infrastructure includes the Maternal-Fetal Pharmacology and Biodevelopment Laboratories, with a state-of-the-art analytical center. Clinical studies are supported by translational projects whic are focused on basic science investigations that will improve clinical outcomes. Our strategy is to leverage and expand our existing resources in order to translate knowledge from basic sciences to new treatments and to translate findings from clinical studies into clinical practice. This strategy will be accomplished by the following specific aims: (1) develop an intellectual, procedural, and physical infrastructure that will accelerate the conduct of clinical trials to determine the efficacy and safety of medications and other therapies as well as support translational projects to determine molecular mechanisms underlying maternal and fetal exposure to medications and biologics; (2) expand the scope of investigation by recruiting new faculty whose expertise will augment the existing multidisciplinary team and by increasing collaboration with UTMB's Maternal Fetal Medicine Units network, Institute for Translational Sciences, and Center for Biomedical Engineering; and (3) increase the number and quality of researchers in the field of maternal-fetal pharmacology by providing training options for postdoctoral and clinical fellows as well as junior faculty via various tracks of hands-on training 1-on-1 mentoring, formal career development programs, didactic multidisciplinary courses, and postgraduate degrees in basic and clinical sciences. We anticipate that collaborations among and beyond the Center's investigative teams will lead to continued opportunities to synergistically translate new hypotheses, research findings, and clinical studies to improve maternal-fetal outcomes.

Public Health Relevance

The goal of this proposal is to establish a center at UTMB for the development of medications and biologics to treat pregnant patients and/or their fetuses. Thematically linked clinical and translational projects will be supported by 2 key components: (1) an existing clinical and translational research infrastructure and (2) an existing team of clinical and research scientists with a track record of successful collaborations.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54HD047891-12
Application #
9119184
Study Section
Special Emphasis Panel (ZHD1)
Program Officer
Tsilou, Katerina
Project Start
2004-07-01
Project End
2020-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
12
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Texas Medical Br Galveston
Department
Obstetrics & Gynecology
Type
Schools of Medicine
DUNS #
800771149
City
Galveston
State
TX
Country
United States
Zip Code
77555
Speidel, Jordan T; Xu, Meixiang; Abdel-Rahman, Sherif Z (2018) Bisphenol A (BPA) and bisphenol S (BPS) alter the promoter activity of the ABCB1 gene encoding P-glycoprotein in the human placenta in a haplotype-dependent manner. Toxicol Appl Pharmacol 359:47-54
Speidel, Jordan T; Xu, Meixiang; Abdel-Rahman, Sherif Z (2018) Promoter Haplotypes of the ABCB1 Gene Encoding the P-Glycoprotein Differentially Affect Its Promoter Activity by Altering Transcription Factor Binding. DNA Cell Biol 37:973-981
Shah, Mansi; Bourner, Luke; Ali, Shariq et al. (2018) HPLC Method Development for Quantification of Doxorubicin in Cell Culture and Placental Perfusion Media. Separations 5:
Speidel, Jordan T; Xu, Meixiang; Abdel-Rahman, Sherif Z (2018) Differential effect of ABCB1 haplotypes on promoter activity. Pharmacogenet Genomics 28:69-77
Al-Enazy, Sanaalarab; Ali, Shariq; Albekairi, Norah et al. (2017) Placental control of drug delivery. Adv Drug Deliv Rev 116:63-72
Marrs, Caroline C; Costantine, Maged M (2017) Should We Add Pravastatin to Aspirin for Preeclampsia Prevention in High-risk Women? Clin Obstet Gynecol 60:161-168
Gopalakrishnan, Kathirvel; More, Amar S; Hankins, Gary D et al. (2017) Postnatal Cardiovascular Consequences in the Offspring of Pregnant Rats Exposed to Smoking and Smoking Cessation Pharmacotherapies. Reprod Sci 24:919-933
Shah, Mansi; Bourner, Luke; Ali, Shariq et al. (2017) Cytotoxicity of Endocytosis and Efflux Inhibitors in the BeWo Cell Line. J Pharm Res Int 17:
Costantine, Maged M; Ananth, Cande V (2016) The early developments of preeclampsia drugs. Expert Opin Investig Drugs 25:867-70
Costantine, Maged M (2016) Pravastatin to prevent obstetrical complications in women with antiphospholipid syndrome. J Clin Invest 126:2792-4

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