Effects of Dual Cyclooxygenase-2 and Carbonic Anhydrase Inhibition

University of Pennsylvania

Status and phase: Terminated; Phase 1

Conditions: Healthy Volunteers

Treatments: Drug: CG100649 (8 mg); Drug: Celecoxib; Drug: CG100649 (2 mg); Drug: Naproxen; Drug: Placebo capsules; Drug: Acetazolamide

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT00780325

807821

Details and patient eligibility

About

Cyclooxygenase-2 (COX-2) inhibitors have become a common analgesic treatment option for patients with arthritis. However, long-term treatment has been associated with increased cardiovascular risk. With the past withdrawals and rejections of approval for COX-2 inhibitors the treatment options are now very limited.

This translates for example to about 10 million osteoarthritis patients in the US who cannot receive COX-2 inhibitors because of concomitant hypertension. And this exemplifies the unmet medical need to develop and offer safe treatment options for this particular patient population.

This trial investigates pharmacodynamic aspects of CG100649 which is being developed as a novel COX-2 inhibitor. Preclinical data show a dual mechanism of action, which consists of the inhibition of the two enzymes COX-2 and carbonic anhydrase-I/-II (CA-I/II) and through which the cardiovascular risk of COX-2 inhibition might be attenuated.

Full description

Part 1 and 2 (staged analysis): Single dose of study drugs [celecoxib, placebo] followed by 3 days of blood draws as Period I; then after a wash-out phase, single dose of study drugs [CG100649 2mg and 8mg, celecoxib 200mg, placebo], followed by blood draws on 6 days and bi-weekly urine collections for 8 weeks.

Part 3: Five-way cross-over of single doses of study drugs with a CG100649 single dose level as determined by part 1 and 2, celecoxib 200mg, naproxen 500mg, acetazolamide 250mg and placebo.

Enrollment: 26 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Age 18-60 years old, able and willing to provide written informed consent to participate in the study;
2. Subjects must be in generally good health as determined by pre-study medical history, physical examination, clinical laboratory tests and 12-lead electrocardiogram (ECG);
3. Body mass index (BMI) 19-32 kg/m2;
4. Normal blood pressure (BP) [systolic BP 90-140 mmHg, diastolic BP 50-90 mmHg] and heart rate (HR) [resting HR 45-90 bpm] without medication;
5. Clinical chemistry profile including electrolytes, alkaline phosphatase (ALK), lactate dehydrogenase (LDH), creatine phosphokinase (CPK), creatinine, and urea must be within the normal range without medication; screening liver enzymes may be up to 1.5x normal range; screening CPK must be within 2x normal range without medication;
6. Urinalysis including urinary creatinine must be within normal limits (trace findings and minor deviations are acceptable per the clinical decision of the Principal Investigator);
7. Subjects must be non-smokers and non-drinkers or willing to abstain from smoking, alcohol, caffeine and high-fat foods for the duration of study;
8. Subjects must be able to read, understand and follow the study instructions;
9. Subjects and their sexual partners must agree to use double barrier contraception during the study period and for 2 months afterward or provide proof of surgical sterility. Double barrier contraception may include, but is not limited to, using a male condom with spermicide; having a female sexual partner who agrees to use an IUD with spermicide, a female condom with spermicide, a diaphragm with spermicide, a cervical cap with spermicide; or having a sterile sexual partner. Female subjects must be non-pregnant, non-lactating, and either postmenopausal for at least 1 year, surgically sterile for at least 3 months, or willing to use double barrier contraception from 28 days prior to study enrollment and/or their last confirmed menstrual period (whichever is longer) until 2 months after final clinic visit. For all females, the pregnancy test result must be negative at Screening;
10. Subjects must tolerate the insertion of an intravenous line of the size ≥ 20 gauge for the drug administration study days.

Exclusion criteria

1. Use of any non-study medication(s) including low dose aspirin for cardiovascular prophylaxis within 2 weeks prior and 2 weeks after receipt of each dose of study drug;
2. Use of chemotherapy agents or history of cancer, other than non-metastatic skin cancer that has been completely excised, within five (5) years prior to the screening visit;
3. History of bacterial or viral infection requiring treatment with antibiotics or antivirals within 3 months of study;
4. Presence or history of peripheral edema within the past 5 years;
5. History of congestive heart failure;
6. Use of drugs which are P450 3A4 inducers or inhibitors within the past 30 days (e.g. alprazolam, chlorpheniramine, cimetidine, fluoxetine, haloperidol, ketoconazole, itraconazole, erythromycin, clarithromycin, sildenafil, simvastatin, St. John's Wort);
7. Use of prescribed systemic or topical medications or any dietary aids or foods that are known to modulate drug metabolizing enzymes (e.g. grapefruit juice) within 14 days of dose administration;
8. Difficulty in swallowing oral medications;
9. History of seizure disorder;
10. Serious psychosocial co-morbidities;
11. Cognitive or psychiatric disorders, or any other condition that could interfere with compliance with study procedures and/or confinement in a clinical study unit for 2 days or longer;
12. History of drug or alcohol abuse within one year prior to screening;
13. Use of any other investigational drug within 1 month prior to enrollment;
14. Use of any prescription drugs within 1 month prior to enrollment;
15. Use of over the counter medication excluding routine vitamins, but including mega-dose vitamin therapy, within one week of enrollment;
16. Donation and/or receipt of any blood or blood products within 3 months prior to enrollment;
17. Active gastrointestinal, renal, hepatic, or coagulant disorder within 1 month prior to enrollment;
18. Esophageal or gastroduodenal ulceration within 1 month prior to enrollment;
19. Hypersensitivity to NSAIDs, sulfonamides, COX-2 inhibitors, or carbonic anhydrase inhibitors;
20. Known allergy or hypersensitivity to sulfa drugs;
21. Family history of significant cardiac disease (i.e. sudden death in first degree relative; myocardial infarction prior to 50 years old);
22. Occult blood in stool (fecal occult blood test).

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Quadruple Blind

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26 participants in 6 patient groups, including a placebo group

1

Experimental group

Description:

CG100649, single oral dose of 2 mg

Treatment:

Drug: CG100649 (2 mg)

2

Experimental group

Description:

CG100649, single oral dose of 8 mg

Treatment:

Drug: CG100649 (8 mg)

3

Active Comparator group

Description:

Celecoxib, single oral dose of 200 mg

Treatment:

Drug: Celecoxib

4

Active Comparator group

Description:

Naproxen, single oral dose of 500 mg

Treatment:

Drug: Naproxen

5

Active Comparator group

Description:

Acetazolamide, single oral dose of 250 mg

Treatment:

Drug: Acetazolamide

6

Placebo Comparator group

Description:

Placebo, single oral administration

Treatment:

Drug: Placebo capsules