Theophylline as a Treatment for Children With Pseudohypoparathyroidism Type 1a (Albright Hereditary Osteodystrophy)

Vanderbilt University Medical Center

Status and phase: Completed; Phase 2

Conditions: Pseudohypoparathyroidism Type 1a; Albright Hereditary Osteodystrophy

Treatments: Drug: Theophylline

Study type: Interventional

Funder types: Other

Identifiers

NCT02463409

IRB 150497

Details and patient eligibility

About

This study will test an investigational drug, theophylline, in children with pseudohypoparathyroidism type 1a (PHP1a). This study involves a 3 day visit to the Vanderbilt Clinical Research Center.

Full description

Study measures will be done at baseline and during a 24h infusion of IV theophylline. Theophylline levels will be drawn to ensure therapeutic dosing and to monitor for toxicity. Measures include laboratory values, response to PTH infusion and resting energy expenditure.

Enrollment: 6 patients

Sex: All

Ages: 10 to 21 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age 10 to 21 years old
2. English proficiency
3. Clinical and genetic diagnosis of PHP1a

Exclusion criteria

1. Use of a PDE inhibitor in the past 30 days
2. History of a seizure disorder unrelated to hypocalcemia
3. History of a cardiac arrhythmia (not including bradycardia)
4. History of hepatic insufficiency
5. AST or ALT >2x upper limit of normal
6. Total bilirubin >1.5 x upper limit of normal (unless patient has a diagnosis of Gilbert's syndrome and no other causes leading to hyperbilirubinemia are identified)
7. Congestive heart failure
8. Cigarette use in the past 30 days
9. Alcohol use within the past 24 hours
10. Current pregnancy
11. Untreated hypothyroidism (defined as free T4 level < 0.6 ng/dL or TSH >10 mcU/mL)
12. Active peptic ulcer disease
13. Fever >101 degrees in the past 24 hours
14. Current use of medications known to effect theophylline levels (listed below)
15. Severe sleep apnea requiring BiPAP

Drugs with clinically significant drug interactions with theophylline:

• Allopurinol
• Cimetidine
• Ciprofloxacin
• Clarithromycin
• Enoxacin
• Ephedrine
• Erythromycin
• Estrogen
• Flurazepam
• Fluvoxamine
• Lithium
• Lorazepam
• Methotrexate
• Midazolam
• Pentoxifylline
• Propranolol
• Rifampin
• Sulfinpyrazone
• Tacrine
• Thiabendazole
• Ticlopidine
• Troleandomycin
• Verapamil

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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6 participants in 1 patient group

Theophylline

Experimental group

Description:

Patients will receive a 24 hour continuous infusion of intravenous theophylline.

Treatment:

Drug: Theophylline