Appeal 2007-0526 Application 10/141,032 prepare a composition meeting claim 20’s interpatient variability limitation (see Specification 23). Thus, by following the suggestions in Edwards for improving inhaled tobramycin formulations such as Vaghefi’s, one of ordinary skill would not only have made particles with the physical properties recited in claim 20, but would also have used preparative methods that result in a composition meeting the interpatient variability limitation in claim 20. We therefore agree with the Examiner that, taken together, Edwards and Vaghefi suggest all the limitations in claim 20. Appellants argue that the “amount of experimentation that would be required for one of ordinary skill in the art to fabricate formulations comprising particles containing any selected one of the hundreds of pharmaceutical agents listed in Vaghefi, using the selected particle fabrication methods taught by Edwards et al., would be undue experimentation” (Br. 13). Appellants urge that the rejection relies on impermissible hindsight to reconstruct the claimed invention (id. at 14). We do not find this argument persuasive. The obviousness of including tobramycin in Edwards’ inhaled powder formulation is not undermined by the fact that Vaghefi includes tobramycin in a large list of other therapeutic agents suitably administered by inhalation. For example, in Merck & Co. v. Biocraft Labs. Inc., 874 F.2d 804, 806-07, 10 USPQ2d 1843, 1845 (Fed. Cir. 1989), the court held a composition obvious despite the fact that the two ingredients in the composition were one of 1200 possible combinations suggested in the prior art. Id. at 807, 10 USPQ2d at 1846 (“That the [reference] discloses a multitude of effective combinations 11Page: Previous 1 2 3 4 5 6 7 8 9 10 11 12 13 14 Next
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