Yoshihiro Fujikawa, Mikio Suzuki, Hiroshi Iwasaki, Mitsuaki Sakashita and Masaki Kitahara v. Sompong Wattanasin, (Two Cases)

Yoshihiro Fujikawa et al. (Fujikawa) appeal from two decisions of the Board of Patent Appeals and Interferences of the United States Patent & Trademark Office (Board) granting priority of invention in two related interferences to Sompong Wattanasin, and denying Fujikawa’s motion to add an additional sub-genus count to the interferences. We affirm.

I

These interferences pertain to a compound and method for inhibiting cholesterol biosyn-thesis in humans and other animals. The compound count recites a genus of novel mevalonolactones. The method count recites a method of inhibiting the biosynthesis of cholesterol by administering to a “patient in need of said treatment” an appropriate dosage of a compound falling within the scope of the compound count.

The real parties in interest are Sandoz Pharmaceuticals Corporation (Sandoz), as-signee of Wattanasin, and Nissan Chemical Industries, Ltd. (Nissan), assignee of Fujika-wa.

The inventive activity of Fujikawa, the senior party, occurred overseas. Fujikawa can thus rely only on his effective filing date, August 20, 1987, to establish priority. 35 U.S.C. § 102(g) (1994). Whether Wattanasin is entitled to priority as against Fujikawa therefore turns on two discrete questions. First, whether Wattanasin has shown conception coupled with diligence from just prior to Fujikawa’s effective filing date until reduction to practice. Id. Second, whether Wat-tanasin suppressed or concealed the invention between reduction to practice and filing. Id. With respect to. the first question, Fuji-kawa does not directly challenge the Board’s holdings on Wattanasin’s conception or diligence, but rather contends that the Board incorrectly fixed the date of Wattanasin’s reduction to practice. As for the second question, Fujikawa contends that the Board erred in concluding that Wattanasin had not suppressed or concealed the invention. Fuji-kawa seeks reversal, and thus to establish priority in its favor, on either ground.

II

The Board divided Wattanasin’s inventive activity into two phases. The first phase commenced in 1979 when Sandoz began searching for drugs which would inhibit the biosynthesis of cholesterol. Inventor Watta-nasin was assigned to this project in 1982, and during 1984-1985 he synthesized three compounds falling within the scope of the compound count. When tested in vitro, each of these compounds exhibited some cholesterol-inhibiting activity, although not all the chemicals were equally effective. Still, according to one Sandoz researcher, Dr. Damon, these test results indicated that, to a high probability, the three compounds “would be active when administered in vivo to a patient to inhibit cholesterol biosynthesis, i.e. for the treatment of hypercholesteremia or atherosclerosis.” Notwithstanding these seemingly positive results, Sandoz shelved Wattanasin’s project for almost two years, apparently because the level of in vitro activity in two of the three compounds was disappointingly low.

By January 1987, however, interest in Wattanasin’s invention had revived, and the second phase of activity began. Over the next several months, four more compounds falling within the scope of the compound count were synthesized. In October, these compounds were tested for in vitro activity, and each of the four compounds yielded positive results. Again, however, there were significant differences in the level of in vitro activity of the four compounds. Two of the compounds in particular, numbered 64-935 and 64-936, exhibited in vitro activity significantly higher than that of the other two compounds, numbered 64-933 and 64-934.

Soon after, in December 1987, the three most active compounds in vitro were subjected to additional in vivo testing. For Sandoz, one primary purpose of these tests was to *1562 determine the m vivo potency of the three compounds relative to that of Compactin, a prior art compound of known cholesterol-inhibiting potency. From the results of the in vivo tests, reproduced in the margin, 1 Sandoz calculated an EDS0 2 for each of the compounds and compared it to the ED50 of Compactin. Only one of the compounds, compound 64-935, manifested a better ED50 than Compactin: an ED5o of 0.49 as compared to Compactin’s ED50 of 3.5. All of the tests performed by Sandoz were conducted in accordance with established protocols.

During this period, Sandoz also began to consider whether, and when, a patent application should be filed for Wattanasin’s invention. Several times during the second phase of activity, the Sandoz patent committee considered the question of Wattanasin’s invention but decided that it was too early in the invention’s development to file a patent application. Each time, however, the patent committee merely deferred decision on the matter and specified that it would be taken up again at subsequent meetings. Finally, in January 1988, with the in vivo testing completed, the Committee assigned Wattanasin’s invention an “A” rating which meant that the invention was ripe for filing and that a patent application should be prepared. The case was assigned to a Ms. Geisser, a young patent attorney in the Sandoz patent department with little experience in the pharmaceutical field.

Over the next several months the Sandoz patent department collected additional data from the inventor which was needed to prepare the patent application. This data gathering took until approximately the end of May 1988. At that point, work on the case seems to have ceased for several months until Ms. Geisser began preparing a draft sometime m the latter half of 1988. The parties dispute when this preparation began. Fujikawa contends that it occurred as late as October, and that Ms. Geisser was spurred to begin preparing the draft application by the discovery that a patent to the same subject matter had been issued to a third party, Picard. Fujikawa, however, has no evidence to support that contention. In contrast, San-doz contends that Ms. Geisser began the draft as early as August, and that she was already working on the draft when she first heard of Picard’s patent. The evidence of record, and in particular the testimony of Ms. Geisser, supports that version of events. In any event, the draft was completed in November and, after several turn-arounds with the inventor, ultimately filed in March of 1989.

Both Wattanasin and Fujikawa requested an interference with Picard. The requests were granted and a three-party interference between Picard, Fujikawa, and Wattanasin was set up. Early in the proceedings, however, Picard filed a request for an adverse judgment presumably because he could not antedate Fujikawa’s priority date. What remained was a two-party interference between Fujikawa and Wattanasin. Ultimately, for reasons not significant to this appeal, the interference was divided into two interferences: one relating to the method count and one relating to the compound count. The Board decided each of these interferences adverse to Fujikawa.

With respect to the compound count, the Board made two alternative findings regarding reduction to practice. First, it found that the in vitro results in October 1987 showed sufficient practical utility for the compound so as to constitute a reduction to practice as of the date of those tests. 3 In the alterna *1563 tive, the Board held, the in vivo tests which showed significant activity in the 64-935 compound at doses of 1.0 and 0.1 mg were sufficient to show practical utility. Consequently, Wattanasin had reduced the compound to practice, at the latest, as of December 1987. Since Fujikawa did not challenge Wattana-sin’s diligence for the period between Fujika-wa’s effective filing date of August 20, 1987 and Wattanasin’s reduction to practice in either October or December 1987, the Board held that Wattanasin was de facto the first inventor of the compound count. Finally, the Board found that the seventeen month period (counting from the in vitro testing) or fifteen month period (counting from the in vivo testing) between Wattanasin’s reduction to practice and filing was not sufficient to raise an inference of suppression or concealment given the complexity of the invention, and therefore awarded priority of the compound count to Wattanasin. In reaching this conclusion, the Board rejected Fujikawa’s argument that Wattanasin was spurred to file by Picard because it held that spurring by Pi-card, a third party, had no legal effect in a priority dispute between Fujikawa and Wat-tanasin.

With respect to the method count, the Board determined that Wattanasin reduced to practice in December 1987 on the date that in vivo testing of the 64-935 compound was concluded. In reaching that conclusion, the Board first noted that a reduction to practice must include every limitation of the count. Consequently, Wattanasin’s early in vitro testing could not constitute a reduction to practice of the method count, since that count recites administering the compound to a “patient.” The in vivo testing, however, met the limitations of the count since the word “patient” was sufficiently broad to include the laboratory rats to whom the compounds were administered. The in vivo testing also proved that 64-935 had practical utility because the compound displayed significant cholesterol inhibiting activity at doses of 1.0 and 0.1 mg. Given this date of reduction to practice, the Board again held that Wattanasin was the de facto first inventor of the count and that the delay in filing of fifteen months was not sufficient to trigger an inference of suppression or concealment. The Board therefore awarded priority of the method count to Wattanasin.

Before this court, Fujikawa seeks review of these adverse priority determinations. In addition, during the motions period of the .interference, Fujikawa moved to have an additional sub-genus count added to the interference. The Board denied that motion on the ground that the Wattanasin disclosure did not contain a sufficient written description to support the proposed count. Fujika-wa appeals that decision, as well. We have jurisdiction to hear this appeal under 28 U.S.C. § 1295(a)(4)(A) (1994).

Ill

We first address Fujikawa’s argument that Wattanasin’s in vitro and in vivo tests failed to establish a practical utility for either the compound or method count. The Board held that the in vitro tests established a practical utility for the compound and that the in vivo tests established a practical utility for both the compound and method counts. For the reasons set out below, we affirm these findings of the Board.

For over 200 years, the concept of utility has occupied a central role in our patent system. See Brenner v. Manson, 383 U.S. 519, 529, 86 S.Ct. 1033, 1039, 16 L.Ed.2d 69, 148 USPQ 689, 693 (1966). Indeed, “[t]he basic quid pro quo contemplated by the Constitution and the Congress for granting a patent monopoly is the benefit derived by the public from an invention with substantial utility.” Id. at 534, 86 S.Ct.at 1042, 148 USPQ at 695. Consequently, it is well established that a patent may not be granted to an invention unless substantial or practical utility for the invention has been discovered and disclosed. See Cross v. Iizuka, 753 F.2d 1040, 1044, 224 USPQ 739, 742 (Fed.Cir.1985). Similarly, actual reduction to practice, which constitutes in law the final phase of invention, cannot be established absent a showing of practical utility. See Blicke v. Treves, 44 C.C.P.A. 753, 241 F.2d 718, 720-21, 112 USPQ 472, 474-75 (1957).

*1564 In the pharmaceutical arts, our court has long held that practical utility may be shown by adequate evidence of any pharmacological activity. See, e.g., Nelson v. Bowler, 626 F.2d 853, 856, 206 USPQ 881, 883 (CCPA 1980); In re Krimmel, 48 C.C.P.A. 1116, 292 F.2d 948, 952-53, 130 USPQ 215, 219 (1961). For example, in Campbell v. Wettstein, 476 F.2d 642, 646-47, 177 USPQ 376, 379 (CCPA 1973) we stated that “[m]oreover, the interference counts contain no limitation relating to intended use or to discovered properties of the claimed compounds. Accordingly, under well-established precedent, evidence establishing substantial utility for any purpose is sufficient to show reduction to practice.” The rule in Campbell was applied in Rey-Bellet v. Engelhardt, 493 F.2d 1380, 1383, 181 USPQ 453, 454 (CCPA 1974) (“Since the count contains no limitation related to any utility, evidence which would establish a substantial utility for any purpose is sufficient to show its reduction to practice.”). 4 Such activity constitutes a practical utility because “[i]t is inherently faster and easier to combat illnesses and alleviate symptoms when the medical profession is armed with an arsenal of chemicals having known pharmacological activities. Since it is crucial to provide researchers with an incentive to disclose pharmacological activities in as many compounds as possible, we conclude that adequate proof of any such activity constitutes a showing of practical utility.” Nelson, 626 F.2d at 856, 206 USPQ at 883; see also Krimmel, 292 F.2d at 952-53, 130 USPQ at 219.

It may be difficult to predict, however, whether a novel compound will exhibit pharmacological activity, even when the behavior of analogous compounds is known to those skilled in the art. Consequently, testing is often required to establish practical utility. See, e.g., Blicke, 241 F.2d at 720, 112 USPQ at 475. But the test results need not absolutely prove that the compound is phar-macologically active. All that is required is that the tests be “reasonably indicative of the desired [pharmacological] response.” Nelson, 626 F.2d at 856, 206 USPQ at 884. (emphasis added). In other words, there must be a sufficient correlation between the tests and an asserted pharmacological activity so as to convince those skilled in the art, to a reasonable probability, that the novel compound will exhibit the asserted pharmacological behavior. See Cross, 753 F.2d at 1050, 224 USPQ at 747.

The ultimate determination of reduction to practice is a question of law which we review de novo. See Holmwood v. Sugavanam, 948 F.2d 1236, 1238, 20 USPQ2d 1712, 1714 (Fed.Cir.1991). In contrast, we review the Board’s factual findings supporting its legal conclusions about reduction to practice for clear error. Id. Whether a practical utility has been established for a novel compound is a question of fact. See Cross, 753 F.2d at 1044 n. 7, 224 USPQ at 742 n. 7. We therefore review the Board’s findings with respect to practical utility for clear error.

A

This court has, on many occasions, considered the type and quantity of testing necessary to establish a practical utility for a novel compound. Although each case of practical utility must be considered on its own facts, see, e.g., Blicke, 241 F.2d at 720, 112 USPQ at 475, examination of our precedent illustrates the degree of proof which we have deemed sufficient to establish practical utility in the past.

The facts in this case are substantially similar to those in Cross v. Iizuka, 753 F.2d 1040, 224 USPQ 739 (Fed.Cir.1985). There, we expressly held that, in appropriate circumstances, evidence of in vitro testing *1565 could adequately establish a practical utility. 5 As we there explained:

We perceive no insurmountable difficulty, under appropriate circumstances, in finding that the first link in the screening chain, in vitro testing, may establish a practical utility for the compound in question.... [U]nder the circumstances of the instant ease, where [an application] discloses an in vitro utility, ... and where the disclosed in vitro utility is supplemented by the similar in vitro and in vivo pharmacological activity of structurally similar compounds, ... we agree with the Board that this in vitro utility is sufficient to [establish utility].

Id. at 1051, 224 USPQ at 748. Thus, Cross holds that positive in vitro results, in combination with a known correlation between such in vitro results and in vivo activity, may be sufficient to establish practical utility.

Fujikawa does not argue that the law as stated in Cross is incorrect. Instead, Fujika-wa contends that Wattanasin has failed to establish an adequate correlation between in vitro and in vivo results in the field of cholesterol-inhibiting compounds to permit Wat-tanasin to rely on affirmative in vitro results to establish a practical utility for the compound.

The Board determined that Wattanasin had reduced the compound count to practice in October 1987 when several compounds falling within the scope of the genus count exhibited activity in vitro. In reaching that conclusion, the Board relied on testimony from those skilled in the art that the in vitro results convinced them that the claimed compounds would exhibit the desired pharmacological activity when administered in vivo. This included testimony that “in vivo activity is typically highly correlatable to a compound’s in vitro activity” in this field. The facts in this case are thus analogous to the ones in Cross where the court relied on positive in vitro test results in combination with a known correlation between such in vitro tests and in vivo activity to support a finding of practical utility.

To counter the Board’s decision, Fujikawa points to the testimony of its own expert, Dr. Holmlund, who testified that:

there is a reasonable element of doubt that some elements may be encountered which are active in the in vitro assay, but yet inactive in the in vivo assay.

According to Fujikawa, this testimony establishes that the in vitro tests were insufficient to prove practical utility.

We note first that to the extent the record presents a conflict in the testimony, the Board was well within its discretion as fact finder to credit the testimony of Wattanasin’s witnesses over that of Fujikawa’s. More fundamentally, however, we do not consider Dr. Holmlund’s testimony as a whole to contradict the Board’s finding. Of course, it is possible that some compounds active in vitro may not be active in vivo. But, as our predecessor court in Nelson explained, a “rigorous correlation” need not be shown in order to establish practical utility; “reasonable correlation” suffices. Here, even Dr. Holmlund implied in the question and answer immediately following the above quoted portion of his testimony, that such a “reasonable correlation” exists:

Q. Would you accept, subject to exceptions that might occur, that the failure to find [in vivo ] activity would be considered an exception, that there would be a reasonable expectancy [that in vitro activity implies that the compound will be active in vivo ]?

A. I think I would probably accept that.

Fujikawa also cites two articles 6 which it claims show that there is no reliable relationship between in vitro results and in vivo results in cholesterol inhibiting compounds similar to the ones at issue in this case. We disagree. Although the Sliskovic article, for *1566 example, teaches that in vitro testing is sometimes not a good indicator of how potent a compound will be in vivo, it does imply that compounds which are active in vitro will normally exhibit some in vivo activity. See Sliskovic, at 370. Similarly, the Kathawala article expressly states: “For most substances, although not for all, the relative potency determined in in vitro microsomal assay against HMG-CoA reductase parallels the in vivo activity in rats for the inhibition of 14C-acetate into sterols.” Kathawala at 136-37. On these facts, we hold that the Board did not err in finding that Wattana-sin’s in vitro tests established a practical utility for the genus recited in the compound count.

B

Turning to the method count, the Board found that Wattanasin reduced the method to practice in December 1987 when successful in vivo testing of the compound was completed. This finding, too, was based on testimony that the in vivo data for one of the compounds tested, 64-935, showed significant cholesterol inhibiting activity in the laboratory rats tested.

Fujikawa challenges the Board’s holding by referring to an anomaly in the test data of the 64r-935 compound which it contends undercuts the reliability of the in vivo tests. In particular, Fujikawa points to the fact that the compound’s potency was less at a dosage of 0.3 mg than it was at a dosage of 0.1 mg. On the basis of this aberration, Fujikawa’s expert, Dr. Holmlund, testified that this test data was unreliable and could not support a finding that the compound was pharmacologi-cally active.

It is clear from the Board’s opinion, however, that to the extent Dr. Holmlund was testifying that this aberration would lead one of ordinary skill to completely reject these test results, the Board did not accept his testimony. This decision of the Board was not clear error. Admittedly, the decreased potency at 0.3 mg is curious. The question remains, however, as to how much this glitch in the data would undercut the persuasiveness of the test results as a whole in the mind of one of ordinary skill. Each party presented evidence on this point and the Board resolved this disputed question of fact by finding that the test results as a whole were sufficient to establish pharmacological activity in the minds of those skilled in the art. In doing so, the Board properly exercised its duty as fact finder, and we therefore affirm its finding on this point. 7

As noted above, Fujikawa does not challenge the Board’s conclusions that Wattana-sin conceived prior to Fujikawa’s effective date or that Wattanasin pursued the invention with diligence from just prior to Fujika-wa’s date until his reductions to practice in October and December 1987. Consequently, we affirm the Board’s finding that Wattana-sin has shown conception coupled with diligence from just prior to Fujikawa’s effective date of August 20, 1987 up to the date he reduced the invention to practice in October 1987, for the compound, or December 1987, for the method.

IV

Having determined that Wattanasin was the de facto first inventor, the remaining question before the Board was whether Wat-tanasin had suppressed or concealed the in *1567 vention between the time he reduced to practice and the time he filed his patent application. Suppression or concealment of the invention by Wattanasin would entitle Fuji-kawa to priority. 35 U.S.C. § 102(g).

Suppression or concealment is a question of law which we review de novo. Brokaw v. Vogel, 57 C.C.P.A. 1296, 429 F.2d 476, 480, 166 USPQ 428, 431 (1970). Ornease law distinguishes between two types of suppression and concealment: cases in which the inventor deliberately suppresses or conceals his invention, and cases in which a legal inference of suppression or concealment is drawn based on “too long” a delay in filing a patent application. Paulik v. Rizkalla, 760 F.2d 1270, 1273, 226 USPQ 224, 226 (Fed.Cir.1985) (in banc).

Fujikawa first argues that there is evidence of intentional suppression or concealment in this ease. Intentional suppression refers to situations in which an inventor “designedly, and with the view of applying it indefinitely and exclusively for his own profit, withholds his invention from the public.” Id. (quoting Kendall v. Winsor, 62 U.S. (21 How.) 322, 328, 16 L.Ed. 165 (1858)). Admittedly, Sandoz was not overly efficient in preparing a patent application, given the time which elapsed between its reduction to practice in late 1987 and its ultimate filing in March 1989. Intentional suppression, however, requires more than the passage of time. It requires evidence that the inventor intentionally delayed filing in order to prolong the period during which the invention is maintained in secret. Cf. Peeler v. Miller, 535 F.2d 647, 653-54, 190 USPQ 117, 122 (CCPA 1976) (implying that intentional suppression requires showing of specific intent). Fujikawa presented no evidence that Wattanasin delayed filing for this purpose. On the contrary, all indications are that throughout the period between reduction to practice and filing, Sandoz moved slowly (one might even say fitfully), but inexorably, toward disclosure. We therefore hold that Wattanasin did not intentionally suppress or conceal the invention in this case.

Absent intentional suppression, the only question is whether the 17 month period between the reduction to practice of the compound, or the 15 month period between reduction to practice of the method, and Wattanasin’s filing justify an inference of suppression or concealment. See id. The Board held that these facts do not support such an inference. As the Board explained: “In our view, this hiatus in time is not sufficiently long to raise the inference that Wat-tanasin suppressed or concealed the invention considering the nature and complexity of the invention here.”

Fujikawa attacks this finding of the Board on two grounds. First, it contends that the Board should not have held that a 15 or 17 month delay is per se insufficient to raise an inference of suppression or concealment without examining the circumstances surrounding the delay and whether, in view of those circumstances, Wattanasin’s delay was reasonable. Second, Fujikawa argues that the Board failed to consider evidence that Wattanasin was spurred to file by the issuance of a patent to a third party, Picard, directed to the same genus of compounds invented by Wattanasin. Evidence that a first inventor was spurred to disclose by the activities of a second inventor has always been an important factor in priority determinations because it creates an inference that, but for the efforts of the second inventor, “the public would never have gained knowledge of [the invention].” Brokaw, 429 F.2d at 480, 166 USPQ at 431. Here, however, the Board expressly declined to consider the evidence of spurring because it held that spurring by a third party who is not a party to the interference is irrelevant to a determination of priority as between Wattanasin and Fujikawa. We first address Fujikawa’s arguments concerning spurring.

A

We are not certain that the Board is correct that third party spurring is irrelevant in determining priority. After all, “[w]hat is involved here is a policy question as to which of the two rival inventors has the greater right to a patent.” Brokaw, 429 F.2d at 480, 166 USPQ at 430. Resolution of this question could well be affected by the fact that one of the inventors chose to maintain his *1568 invention in secrecy until disclosure by another spurred him to file, even when the spurrer was a third party not involved in the interference. We need not resolve that question here, however, because we hold that no reasonable fact finder could have found spurring on the facts of this case. The only evidence in the record on the question of spurring is the testimony of Ms. Geisser who expressly testified that she had already begun work on the Wattanasin draft application before she learned of Picard’s patent, in other words, that she had not been spurred by Picard. Consequently, we leave the question of the relevance of third party spurring for another case.

B

Fujikawa’s other argument also requires us to examine the evidence of record in this ease. As Fujikawa correctly notes, this court has not set strict time limits regarding the minimum and maximum periods necessary to establish an inference of suppression or concealment. See Correge v. Murphy, 705 F.2d 1326, 1330, 217 USPQ 753, 756 (Fed.Cir.1983). Rather, we have recognized that “it is not the time elapsed that is the controlling factor but the total conduct of the first inventor.” Young v. Dworkin, 489 F.2d 1277, 1285, 180 USPQ 388, 395 (CCPA 1974) (Rich, J., concurring). Thus, the circumstances surrounding the first inventor’s delay and the reasonableness of that delay are important factors which must be considered in deciding questions of suppression or concealment. See, e.g., id. at 1281-82, 180 USPQ at 392-93. Fujikawa again correctly notes that the Board’s opinion gives short shrift to the question of whether this delay on the facts of this case was reasonable. In seeking reversal of the Board’s decision, Fujikawa asks us to assess the factual record for ourselves to determine whether Wattanasin engaged in sufficient disclosure-related activity to justify his 17-month delay in filing. The facts of record, however, do not support Fujikawa’s position.

In our view, the circumstances in this ease place it squarely within the class of cases in which an inference of suppression or concealment is not warranted. We acknowledge, of course, that each case of suppression or concealment must be decided on its own facts. Still, the rich and varied case law which this court has developed over many years provides some guidance as to the type of behavior which warrants an inference of suppression or concealment. See Paulik, 760 F.2d at 1280, 226 USPQ at 231-32 (Rich, J., concurring). In this case Wattanasin delayed approximately 17 months between reduction to practice and filing. During much of that period, however, Wattanasin and San-doz engaged in significant steps towards perfecting the invention and preparing an application. For- example, we do not believe any lack of diligence can be ascribed to Wattanasin for the period between October and December 1987 when in vivo testing of the invention was taking place. See Young, 489 F.2d at 1281, 180 USPQ at 392. Similarly, at its first opportunity following the in vivo testing, the Sandoz patent committee approved Wattanasin’s invention for filing. This takes us up to the end of January 1988.

Over the next several months, until May 1988, the Sandoz patent department engaged in the necessary collection of data from the inventor and others in order to prepare Wat-tanasin’s patent application. We are satisfied from the record that this disclosure-related activity was sufficient to avoid any inference of suppression or concealment during this period. 8 Cf. Correge, 705 F.2d at 1330-31, 217 USPQ at 756 (five significant acts of disclosure-related activity over the course of seven months sufficient to rebut any inference of suppression). Also, as noted above, the record indicates that by August 1988, Ms. Geisser was already at work preparing the application, and that work continued on various drafts until Wattanasin’s filing date in March 1989. Thus, the only real period of unexplained delay in this case is the *1569 approximately three month period between May and August of 1988.

Given a total delay of 17 months, an unexplained delay of three months, the complexity of the subject matter at issue, and our sense from the record as a whole that throughout the delay Sandoz was moving, albeit slowly, towards filing an application, we conclude that this case does not warrant an inference of suppression or concealment. Consequently, we affirm the Board on this point.

C

Finally, Fujikawa contends that assuming in vitro tests are sufficient to establish reduction to practice, Wattanasin reduced the compound count to practice in 1984 when he completed in vitro testing of his first three compounds falling within the scope of the count. If so, Fujikawa argues, the delay between reduction to practice and filing was greater than four years, and an inference of suppression or concealment is justified. 9

We reject this argument in view of Paulik v. Rizkalla, 760 F.2d 1270, 226 USPQ 224 (Fed.Cir.1985) (in banc). In Paulik, we held that a suppression or concealment could be negated by renewed activity prior to an opposing party’s effective date. There, inventor Paulik reduced his invention to practice and submitted an invention disclosure to his employer’s patent department. For four years the patent department did nothing with the disclosure. Then, just two months before Rizkalla’s effective date, the patent department allegedly picked up Paulik’s disclosure and worked diligently to prepare a patent application which it ultimately filed. See id. at 1271-72, 226 USPQ at 224-25. We held that although Paulik could not rely on his original date of reduction to practice to establish priority, he could rely on the date of renewed activity in his priority contest with Rizkalla. In large measure, this decision was driven by the court’s concern that denying an inventor the benefit of his renewed activity, might “discourage inventors and their supporters from working on projects that had been ‘too long’ set aside, because of the impossibility of relying, in a priority contest, on either their original work or their renewed work.” Id. at 1275-76, 226 USPQ at 227-28.

Paulik’s reasoning, if not its hold