The Effect of Sulfasalazine on CRH Levels in Pregnant Women

Preterm Birth Clinical Trial

Official title:

The Effect of Sulfasalazine on CRH Levels in Pregnant Women With a History of Pre-Term Birth: A Randomized Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05703425
• Other study ID #: Pro2021001951
• Status: Recruiting
• Phase: Phase 2
• Start date: March 1, 2023
• Est. completion date: June 30, 2026

Study information

• Verified date: April 2024
• Source: Rutgers, The State University of New Jersey
• Contact: Shama Khan, MS
• Phone: 732-407-6421
• Email: khansp[@]rwjms.rutgers.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this randomized clinical trial is to assess sulfasalazine as a potential treatment to prevent recurrent preterm birth. The main questions it aims to answer are:

• Does sulfasalazine down regulate corticotropin releasing hormone (CRH) levels in pregnant persons with a prior history of preterm birth?

• Does sulfasalazine reduce the incidence of recurrent preterm birth in pregnant persons given drug vs. controls?

Consenting participants will be randomized to receive sulfasalazine or to a control group and will undergo serial blood draws to assess plasma CRH levels.

Description:

This is a study to assess the potential for sulfasalazine to prevent recurrent preterm birth. The investigators' main objective is to assess the effects of sulfasalazine on the maternal serum biomarker CRH, which is associated with preterm birth.

The will be a pilot randomized controlled trial of pregnant multiparous patients who have had a prior preterm delivery. Pregnant women with a prior preterm birth are at high risk (about 20-30%) of having a recurrent preterm birth. The goal of the study will be to evaluate the effect of sulfasalazine on the maternal serum biomarker CRH at 28, 32, and 36 weeks gestation after randomization of patients to the study drug.

Secondary objectives include evaluating the effect of sulfasalazine on the outcome of delivery less than 37 weeks gestation in this group of high risk pregnant women. Additional composite neonatal outcomes will be assessed.

The proposed study has the potential to identify a novel, low-cost, orally available treatment for preterm delivery based on in vitro evidence and epidemiologic studies suggesting that sulfasalazine may be an effective intervention to prevent preterm birth. If the hypothesis put forth by the investigators is confirmed, sulfasalazine would be an attractive therapeutic intervention that could be implemented for the prevention of preterm birth in both developed and developing nations.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: June 30, 2026
• Est. primary completion date: January 31, 2026
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• > 18 years of age

• Singleton pregnancy

• Participants with a history of prior preterm birth in a previous pregnancy

• Participants must be between 12 and 22 weeks gestation.

• Participants must have their pregnancy dates confirmed by ultrasound.

Exclusion Criteria:

• Participants < 18 years old

• Participants with a cervical length < 25 mm

• Participants with a multiple gestation

• Cerclage

• Progesterone administration

• Unwilling or unable to swallow the study agent capsule or consume an inert ingredient in the study agent capsule

• Acute liver disease or known liver abnormalities

• Other significant chronic medical or psychiatric illness that, in the investigator's opinion, would prevent participation in the study

• Known hypersensitivity to sulfasalazine

• Known glucose-6-phosphate dehydrogenase (G6PD) deficiency

• History of severe asthma

• Digoxin use

• Porphyria

• Intestinal obstruction

• Urinary tract obstruction

• Hepatic dysfunction

• Renal dysfunction

• Blood dyscrasia such as agranulocytosis, aplastic anemia.

Related Conditions & MeSH terms

• Premature Birth
• Preterm Birth

Intervention

Drug:
• Sulfasalazine
Sulfasalazine will be administered between 24 and 36 weeks of pregnancy

Locations

Country	Name	City	State
United States	Rutgers Robert Wood Johnson Medical School	New Brunswick	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
Rutgers, The State University of New Jersey

Country where clinical trial is conducted

United States, 

References & Publications (6)

Hensleigh PA, Kauffman RE. Maternal absorption and placental transfer of sulfasalazine. Am J Obstet Gynecol. 1977 Feb 15;127(4):443-4. doi: 10.1016/0002-9378(77)90510-5. No abstract available. — View Citation

McLean M, Bisits A, Davies J, Woods R, Lowry P, Smith R. A placental clock controlling the length of human pregnancy. Nat Med. 1995 May;1(5):460-3. doi: 10.1038/nm0595-460. — View Citation

Mogadam M, Dobbins WO 3rd, Korelitz BI, Ahmed SW. Pregnancy in inflammatory bowel disease: effect of sulfasalazine and corticosteroids on fetal outcome. Gastroenterology. 1981 Jan;80(1):72-6. — View Citation

Norgard B, Fonager K, Pedersen L, Jacobsen BA, Sorensen HT. Birth outcome in women exposed to 5-aminosalicylic acid during pregnancy: a Danish cohort study. Gut. 2003 Feb;52(2):243-7. doi: 10.1136/gut.52.2.243. — View Citation

Wang B, Parobchak N, Martin A, Rosen M, Yu LJ, Nguyen M, Gololobova K, Rosen T. Screening a small molecule library to identify inhibitors of NF-kappaB inducing kinase and pro-labor genes in human placenta. Sci Rep. 2018 Jan 26;8(1):1657. doi: 10.1038/s41598-018-20147-0. — View Citation

Wang B, Parobchak N, Rosen T. RelB/NF-kappaB2 regulates corticotropin-releasing hormone in the human placenta. Mol Endocrinol. 2012 Aug;26(8):1356-69. doi: 10.1210/me.2012-1035. Epub 2012 Jun 25. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Serum CRH levels	CRH will be assessed at 28, 32, and 36 weeks gestation	between 28 and 36 weeks of pregnancy
Secondary	Spontaneous preterm birth < 37 weeks gestation	Preterm births prior to 37 weeks secondary to preterm labor (PTL) or premature Preterm births secondary to preterm labor or preterm rupture of the membranes (PPROM)	up to 37 weeks of pregnancy
Secondary	Spontaneous preterm birth < 34 weeks gestation	Preterm births prior to 34 weeks secondary to PTL or PPROM	up to 34 weeks of pregnancy
Secondary	Medically indicated preterm birth < 37 weeks gestation	Preterm births due to maternal or fetal disease not related to PTL or PPROM	up to 37 weeks of pregnancy
Secondary	Digital cervical exam at 36 weeks gestational age	Digital cervical exam at 36 weeks gestational age	between 35 weeks and 36 weeks 6 days of pregnancy
Secondary	Composite neonatal morbidity	Composite outcome including but not limited to Apgar neonatal death, respiratory distress, necrotizing enterocolitis, and bronchopulmonary dysplasia.	From birth of the neonate until 28 days of life