1. Gastrointestinal Review Highlights of the VIGOR Trial Lawrence Goldkind M.D.

2. Outline of Presentation Study hypothesis and definitions of endpoints Review of results High risk populations Review of meta-analysis of phase IIb and III studies presented by the sponsor Conclusions

3. VIGOR Study Design Organ-specific endpoints – PUB’s (Perforation, Symptomatic Ulcers, Bleeding) – Complicated PUB’s (excludes only symptomatic ulcers) Statistical plan : All patients will be followed until: Minimum 120 confirmed PUBs or 40 confirmed complicated PUBs and 6 months after last patient randomized 95% power (  = 0.05 two-tailed) to detect a reduction in risk of at least 50% for the the primary GI hypothesis. –

4. Primary study hypotheses “The risk of confirmed PUBs during the treatment period will be reduced in the group of patients with rheumatoid arthritis taking 50 mg Vioxx daily, compared to the group of patients with rheumatoid arthritis taking naproxen 1000 mg daily. Vioxx administered at a dose of 50 mg daily will be safe and well tolerated.”

5. Endpoint definitions PUB (perforation, symptomatic ulcer, bleed) Complicated PUB

6. Confirmed Event PUB Any one of the following four clinical presentations 1. Ulcer: radiographic, endoscopic, surgical (identified based on clinical presentation including pain as the sole symptom/sign) 2. Perforation: radiographic, endoscopic, surgical, autopsy 3. Obstruction: postprandial nausea and vomiting and evidence of narrowing of the gastric outlet

7. Confirmed Event PUB (continued) 4. Upper GI hemorrhage: Health care provider witnessed: a. frank hematemesis b. coffee ground emesis c. NG aspiration of blood or coffee ground appearing gastric contents d. melena (distinguished from other causes of dark stool) e. Active UGI bleeding at endoscopy, surgery or angiography

8. Confirmed Event PUB (continued) OR Heme-positive stool/ patient reported melena or hematemesis associated with a documented UGI lesion judged by a healthcare provider to be the source of bleeding and associated with significant bleeding* or stigmata of recent bleeding at endoscopy *decrease of > 2 g/dl Hgb, orthostasis, hypotension, transfusion

9. Confirmed Complicated Event PUB Perforation Obstruction GU or DU associated with significant bleeding* *decrease of > 2 g/dl Hgb, orthostasis, hypotension, transfusion

10. Results

11. Confirmed PUB’s in VIGOR N n rate 1 rate 2 Rofecoxib (4047) 56 2.08 1.8% Naproxen (4027) 121 4.49 3.87% Relative Risk: 0.46 p<0.001* * cox proportional hazard model 1 Per 100 PYR. 2 cumulative rate

12. Confirmed Complicated PUBs N n rate 1 rate 2 Rofecoxib (4047) 16 0.59 0.52 % Naproxen (4027) 37 1.37 1.22 % Relative Risk: 0.43 p=0.005* * cox proportional hazard model 1 Per 100 PYR. 2 cumulative rate

13. Types of Confirmed PUBs

14. Subanalysis by Risk factor Prior history of PUB

15. Subanalysis by Risk factor Age

16. High risk populations If age and history of PUB are independent risk factors for ulcer disease...Findings of high risk in association with a therapy may represent intrinsic risk rather than drug effect (no causality) ? OR Interaction between underlying and drug related risk may produce an exaggerated/ higher risk attributable to therapy (causality) ?

17. High risk populations Outstanding question Should high risk patients be treated with “lower relative GI risk” NSAIDs……. or does overall residual GI risk continue to represent a relative contraindication for these patients? Usage implications

18. GI Risk in special populations Other questions GI Risk of co-administration of aspirin and Vioxx: data needed GI Risk of co-administration of aspirin and Vioxx in the elderly: data needed GI risk in elderly with a history of PUB ?

19. Generalizability of GI Safety Relative Risk: Vioxx < naproxen Degree of Absolute risk : data needed Relative Risk compared to other NSAIDs: data needed

20. Data from phase IIb and III studies Meta-analysis of PUBs “Vioxx vs NSAIDs” Three doses of Vioxx: 12.5 mg, 25 mg, 50 mg Two comparators: ibuprofen, diclofenac Duration: 12-52 weeks

21. Data from phase IIb and III studies Meta-analysis of PUBs “Vioxx vs NSAIDs” N Duration* (weeks) Vioxx 12.5 mg: 1209 52 Vioxx 25 mg: 1603 52 Vioxx 50 mg: 545 12 Ibuprofen: 590 12 Diclofenac: 847 52 * at least 200 subjects present at the end of the interval

22. Meta-analysis of cumulative PUB IIb and III Studies

23. Conclusion of meta-analysis of phase IIb and III studies Vioxx dose and duration of exposure affect associated rates Ibuprofen and diclofenac did not perform similarly NSAID as a composite comparator may not be appropriate Meta-analyses combining heterogeneous groups may be problematic

24. Overall Conclusions Vioxx 50 mg associated with a lower rate of symptomatic and complicated ulcers compared to Naproxen 1000 mg in patients with RA not requiring low dose aspirin use ( relative risks 0.46, 0.43) Risk reduction extends across high risk groups

25. Overall Conclusions High risk groups: elderly and those with history of prior PUB continue to have a significant absolute risk of PUBs Generalizability of GI risk reduction to patients requiring low dose aspirin ? Generalizability to other/all traditional NSAIDs ?