IP Library Granted Patent US 8,367,647
Granted Patent B2
US 8,367,647 · App. 12/664,982 · Granted Feb 5, 2013

Treatment of meconium aspiration syndrome with estrogens

Inventors: Herman Jan Tijmen Coelingh Bennink (Werkhoven, NL); Monique Visser (Zeist, NL)
Assignee: Pantarhei Bioscience B.V.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,367,647
App. No.
12/664,982
Granted
Feb 5, 2013
Kind
B2
Abstract

One aspect of the present invention relates to the use of an estrogen in the treatment of Meconium Aspiration Syndrome (MAS) in a newborn infant, said treatment comprising administering an effective amount of estrogen to said newborn infant within 7 days after birth. The present treatment offers the advantage that estrogens can be administered using non-invasive modes of administration, e.g. oral or rectal administration. Other aspects of the present invention relate to a suppository for use in newborn infants comprising at least 1 μg of estrogen and to an oral applicator comprising a container holding an aqueous liquid containing micronised estetrol and a metering dispenser for metering the liquid into the oral cavity of a newborn infant.

Claims (14)

1. A method of treating Meconium Aspiration Syndrome (MAS) in a newborn infant, said method comprising administering an effective amount of estrogen to said newborn infant within 7 days after birth, wherein the estrogen is selected from the group consisting of estetrol, estriol, estradiol and combination thereof.

2. The method according to claim 1 , wherein the estrogen is administered within 1 day after birth.

3. The method according to claim 1 , wherein the estrogen is administered within 6 hours after birth.

4. The method according to claim 1 , wherein the estrogen is administered within 1 hour after birth.

5. The method according to claim 1 , wherein the estrogen administration is discontinued within 90 days after birth.

6. The method according to claim 1 , wherein the estrogen administration is discontinued within 30 days after birth.

7. The method according to claim 1 , wherein the estrogen is administered orally, rectally or by injection.

8. The method according to claim 7 , wherein the estrogen is administered orally or rectally.

9. The method according to claim 8 , wherein the estrogen is administered rectally.

10. The method according to claim 1 , wherein the estrogen is administered to prophylactically treat severe complications of MAS.

11. The method according to claim 1 , wherein the newborn infant exhibits symptoms of chemical pneumonia.

12. The method according to claim 1 , wherein the newborn infant is suffering from hypoxia.

13. The method according to claim 1 , wherein the estrogen is administered in an amount equivalent to an oral dosage of at least 0.1 mg estetrol.

14. The method according to claim 13 , wherein the estrogen comprises at least estetrol.

Assignments (4)
CHANGE OF NAME Recorded Feb 16, 2022
From: ESTETRA SPRL
To: ESTETRA SRL
Reel/Frame 059167/0379 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 11, 2020
From: DONESTA BIOSCIENCE B.V.
To: ESTETRA SPRL
Reel/Frame 051777/0010 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2015
From: PANTARHEI BIOSCIENCE B.V.
To: DONESTA BIOSCIENCE B.V.
Reel/Frame 035632/0119 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2009
From: COELINGH BENNINK, HERMAN JAN TIJMEN; VISSER, MONIQUE
To: PANTARHEI BIOSCIENCE B.V.
Reel/Frame 023716/0273 →
Priority Claims (1)
EP 07110768 · Jun 21, 2007 · regional
Continuity (1)
Related Publication 20100184736A1 · Jul 22, 2010