T 2154/14 (Daptomycin II/CUBIST PHARMACEUTICALS) 29-03-2017

Main request

Priority (Article 87(1) EPC 1973)

Entitlement to priority from P1 - claim 1

1. Claim 1 is drawn up in the so-called Swiss-type format and concerns a dosage regimen - 3 to 10 mg/kg once every 24 hours - for treating a bacterial infection in a human patient with the antibiotic daptomycin (see section IX). The opposition division held that the dose range "3 to 10 mg/kg" was not directly and unambiguously derivable from the first priority application, P1 (see decision under appeal, point 3.2).

2. According to established case law, the requirement for validly claiming priority of "the same invention", referred to in Article 87(1) EPC 1973, means that priority of a previous application in respect of a claim in a European patent application in accordance with Article 88 EPC is to be acknowledged only if the skilled person can derive the subject-matter of the claim directly and unambiguously, using common general knowledge, from the previous application as a whole (cf. opinion G 2/98 of the Enlarged Board of Appeal, OJ EPO 2001, 413, headnote).

3. The appellant submitted that (i) the range of 3 to 10 mg/kg daptomycin was derivable from the explicitly disclosed range of 2 to 10 mg/kg daptomycin in P1, in line with opinion G 2/98 (supra, see Reasons, point 8.4) and further confirmed by decision G 1/15 of the Enlarged Board of Appeal (see Reasons, point 5.1.2). The appellant further submitted that (ii) P1 also provided a basis for the combination of the range of 3 to 10 mg/kg daptomycin with the dosage interval of once every 24 hours.

4. In the following the board will first concentrate on the second part of appellant's argument.

5. P1 reports on studies carried out in dogs to understand the factors governing the muscle toxicity produced by daptomycin. P1 concludes from the dog studies that the frequency of administration is an important variable in determining the muscle toxicity of daptomycin and that, rather than being strictly related to the dose level, the degree of muscle damage appears to be related to the time between treatments (see page 2, second paragraph).

6. As regards the implications of these findings for clinical dosing P1 states that "the findings described above suggest that longer intervals between doses of daptomycin (i.e. once every 12 hours to 24 hours) will minimize the possibility of muscle toxicity in the clinical setting and may permit the use of higher doses than have been possible so far" (see page 2, third paragraph).

7. P1 also discloses that in terms of clinical efficacy, which appears to be related to the peak serum level attained, larger doses of daptomycin should be administered less frequently as opposed to smaller doses more frequently (see page 2, third paragraph).

8. Therefore, P1 discloses to the skilled person that there is a functional relationship between the dose of daptomycin and the dosing interval in terms of safety as regards the problem of skeletal muscle toxicity caused by the antibiotic (see points 5 and 6) and in terms of efficacy in treating the bacterial infection (see point 7). It follows that in a dosage regimen the dose of daptomycin and the frequency of its administration are not independent variables but are functionally linked.

9. As regards administration to humans, P1 discloses that "daptomycin is administered to a patient in need of such treatment at a dose of between 2 and 10 mg/kg and subsequently, re-administering that same dose at intervals between 12 and 24 hours" (see page 2, fourth paragraph).

10. To the skilled person, aware of the functional relationship between the dose of daptomycin and the dosing interval, the disclosed combination of the dose range of 2 to 10 mg/kg daptomycin with a range of dosage intervals of between 12 and 24 hours therefore does not clearly and unambiguously disclose that the lower end of the dose range, e.g. 2 mg/kg of daptomycin, is not only safe but also efficacious to treat a bacterial infection if only administered once every 24 hours. Accordingly, the combination of the dose range of 2 to 10 mg/kg daptomycin with the dosage interval of once every 24 hours is not directly and unambiguously derivable from P1.

11. The appellant submitted that longer administration was highlighted in P1 and that P1 thus provided a pointer to administration of daptomycin once every 24 hours in humans.

12. The board is not persuaded by this line of argument.

P1 explicitly discloses longer intervals to be "once every 12 hours to 24 hours", and thus does not disclose an interval of 24 hours only (see point 6). Therefore, P1 provides no pointer to a dosage interval of 24 hours and thus also not to the combination of the dose range of 2 to 10 mg/kg daptomycin with the dosage interval of once every 24 hours.

13. The board concludes from the above that there is no clear and unambiguous disclosure in P1 of the combination of the dose range of 2 to 10 mg/kg of daptomycin with a dosage interval of "once every 24 hours" and that for that reason alone the subject-matter of claim 1 is not entitled to priority from P1.

14. Therefore, it need not be decided whether or not the first part of appellant's argument, i.e. that the dose range of 3 to 10 mg/kg of daptomycin is disclosed in P1, is correct.

Entitlement to priority from P2 - claim 1

15. The opposition division decided that page 5, lines 1 to 2, of P2 disclosed the subject-matter of claim 1 and that the effective date for claim 1 was thus the filing date of P2 (see decision under appeal, points 3.3 and 3.4). The respondents contested this part of the decision. In the board's view, the question whether or not page 5, lines 1 to 2, of P2 discloses the claimed subject-matter can be left open if there are other passages in P2 which do disclose the subject-matter of claim 1.

16. Claim 1 of P2 discloses "administering to a patient in need thereof a therapeutically effective amount of daptomycin in a dose of 2 to 75 mg/kg of daptomycin, wherein the daptomycin is administered once every 12 to 24 hours." Dependent claim 2 defines the dose to be

"2 to 10 mg/kg" while claim 3, which depends on claim 2, defines the dose to be "3, 4, 5, 6, 7, 8 or 9 mg/kg". Claim 4 depends on claim 2 and defines that "daptomycin is administered once every 24 hours".

17. In the board's opinion, the skilled person recognises the value 3 mg/kg of daptomycin in claim 3 as a singularity within or at the end of a range of possibilities, which value may therefore mark an end-point for a particular sub-range (cf. decision T 201/83, OJ EPO 1984, 481, Reasons, points 8 and 9). Following the reasoning developed in decision T 201/83 (supra, Reasons, point 12) the broader range of 2 to 10 mg/kg daptomycin recited in claim 2 of P2 in combination with the disclosure of the specific value 3 mg/kg in claim 3 of P2 thus discloses directly and unambiguously the sub-range of 3 to 10 mg/kg daptomycin.

18. From the description of P2 the skilled person learns that the data obtained in two dog studies "suggest that dosing interval had a greater influence on muscle toxicity than did dose itself" (see page 3, lines 24 to 29), and further that "studies in animal efficacy models have demonstrated that effectiveness of daptomycin is optimized by once-daily dosing" (sentence bridging pages 3 and 4) and that "these results suggest that once-daily dosing can minimize daptomycin muscle toxicity, while optimizing its antimicrobial efficacy" (see page 4, lines 2 to 4). In the board's view, the description of P2 thus puts a clear emphasis on once-daily dosing of daptomycin. Also according to claim 4 of P2, which is dependent on claim 2, daptomycin "is administered once every 24 hours". The combination of the range of 3 to 10 mg/kg daptomycin with the specific dosage interval of once every 24 hours is thus directly and unambiguously derivable from the description of P2 and is further confirmed by dependent claim 4 of P2 which provides a clear emphasis on the 24-hour dosage interval.

19. The respondents also submitted that P2 did not disclose that a dose of 3 mg/kg daptomycin was also therapeutically effective if given once daily.

20. However, claim 1 relates to a therapeutically effective amount of daptomycin which includes also 3 mg/kg.

Dependent claim 2 narrows the dose to 2 to 10 mg/kg of daptomycin and according to claim 4, which depends on claim 2, administration is once every 24 hours. Accordingly, P2 discloses that a dose of 3 mg/kg daptomycin is therapeutically effective if given once daily.

21. The board concludes from the above that the subject-matter of claim 1 is entitled to priority from P2 when read as a whole, in particular in combination with the subject-matter as defined in claims 1 to 4.

Conclusion as regards entitlement to priority - claim 1

22. The subject-matter of claim 1 is not entitled to priority from P1 but is entitled to priority from P2. The effective date of the subject-matter of claim 1 of the main request is thus the filing date of P2, i.e. 24 March 1999.

Document D13 - availability to the public

23. Document D13 consists of one page of abstracts, including abstract No. 1520 entitled "Once-daily dosing decreases toxicity of daptomycin". The opposition division considered that, for the subject-matter of claim 1, the effective date of which was the filing date of P2, document D13 belonged to the state of the art within the meaning of Article 54(2) EPC 1973 (see decision under appeal, point 4.2). The appellant disputed that document D13 or its content was available to the public before 24 March 1999.

24. Document D13 does not bear a publication date or date stamp. At the bottom of the page the page number, "322", is indicated followed by "SOT 1999 Annual Meeting". At the very bottom of the document, the statement "Supplied by The British Library - 'The world's knowledge'" is printed. From document D13 itself it is thus not apparent whether or not it was published before 24 March 1999.

25. The respondents relied on two further documents, D26 and D28, to establish the date on which the content of document D13 became available to the public.

Document D26, an extract from a supplement of The Toxicologist (see pages 1 and 2), discloses on page 3 that "this issue of The Toxicologist is devoted to the abstracts of the presentations for the symposium, platform, poster/discussion, workshop, roundtable, and poster sessions of the 38**(th) Annual Meeting of the Society of Toxicology, held at the Ernest N. Morial Convention Center, New Orleans, Louisiana, March 14-18, 1999" (see first paragraph) and that "the abstracts are reproduced as accepted by the Program Committee of the Society of Toxicology and appear in numerical sequence" (fourth paragraph). The fourth page of document D26 bears the page number "322" and is identical to document D13, with the sole difference that the statement at the bottom of the page which reads "Supplied by The British Library - 'The world's knowledge'" is absent.

26. In the board's view, document D26 establishes that the content of document D13 formed part of the abstracts volume of The Toxicologist. The board has no reason to doubt that page 4 of document D26 belongs to the abstracts volume of The Toxicologist: "SOT" is obviously the abbreviation for "Society of Toxicology" (see also e.g. page 10 of document D28) and a clear reference to the annual meeting in 1999 is given on page 4 of document D26 itself. That document D13 contains the additional statement "Supplied by The British Library..." at the very bottom is not in contradiction to page 4 of document D26 since the appearance of document D13 suggests that the latter is a photocopy of a paper document with the additional statement added to the copied original. That document D13 was supplied by the British Library while document D26 was not has no bearing on the issue to be decided, namely the public availability of the content of document D13.

27. Document D28, an extract of the Program of the 38th Annual Meeting of the Society of Toxicology held on 14 to 18 March 1999 (see page 1) discloses on the page bearing page number 6 (page 10 of the document) under the heading "Receipt of the Program and The Toxicologist" that: "1. SOT members in the U.S. and Canada will receive the Program and The Toxicologist (abstracts volume) prior to the meeting as will U.S. and Canadian members who pre-register by January 11, 1999. 2. SOT members and non-member pre-registrants outside the US and Canada, as well as non-members in the U.S. who register after January 11, will receive the Program and The Toxicologist at the registration desk on-site(...) Note: Please bring your copy of the Program and The Toxicologist with you to the meeting."

28. In the board's view, document D28 thus establishes when the abstracts volume of The Toxicologist and thus also the content of document D13 became available to the public.

29. The appellant submitted that no link between document D28 and document D26 had been established.

30. However, the board notes that document D28 contains under the heading "Poster Sessions" inter alia a reference to abstract Nos. 1500-1540 (see page numbered 20/page 24 of D28, right-hand column). The title and the authors of abstract No. 1520 disclosed in document D28 (see page 36 of D28, in the middle of the right-hand column) correspond to the title and authors given on page 4 of document D26 for abstract No. 1520. The board is thus convinced that document D26 is an extract from the abstract volume of The Toxicologist referred to in document D28.

31. Based on the evidence presented to it, the board thus concludes that the content of document D13 became available to the public at the latest as of the first day of the 1999 Annual Meeting of the Society of Toxicology, i.e. 14 March 1999, in the form of a written abstract contained within the abstracts volume of The Toxicologist (see points 25 and 26) handed out at the registration desk to the attendees of the 1999 Annual Meeting (see points 27 and 28). Its content therefore forms part of the state of the art within the meaning of Article 54(2) EPC 1973 for the subject-matter of claim 1.

Inventive step (Article 56 EPC 1973)

32. The opposition division had held that document D8 represented the closest prior art for the claimed invention and that the claimed subject-matter was obvious in view of document D8 in combination with the teaching of document D13 and/or document D1 (see decision under appeal, reasons, points 6.1 to 6.4).

33. On appeal, the parties disagreed on which document represented the closest prior art. While the appellant submitted that document D1 was the closest prior art, the respondents maintained that document D8 represented the closest prior art.

34. In accordance with established jurisprudence, the closest prior art for assessing inventive step is normally a prior-art document disclosing subject-matter conceived for the same purpose or aiming at the same objective as the claimed invention and having the most relevant technical features in common, i.e. requiring the minimum of structural modifications (see Case Law of the Boards of Appeal of the EPO, 8th edition 2016, section I.D.3.1).

35. The purpose of the claimed invention is the treatment of a bacterial infection in a human patient. According to paragraph [0010] of the patent the invention addresses the problem of skeletal muscle toxicity at high doses of daptomycin and provides for the use of the antibiotic in a manner that minimises skeletal muscle toxicity while simultaneously maintaining a sufficient efficacy level.

36. Document D1 discloses that "daptomycin is bactericidal in Gram-positive pathogens, including enterococci (...), and the rate of killing is dose-dependent" (see page 420, fourth paragraph, line 7). Document D1 also reviews the clinical trials that have been carried out on daptomycin in human patients (see page 423, last paragraph, to page 424, third paragraph). It discloses that "at a dose of 2 mg/kg every 24 hr, daptomycin was shown to be effective in treating a variety of Gram-positive infections" (see page 424, lines 5 to 6) and that "in another study, daptomycin given at a dose of 3 mg/kg every 12 hr was shown to be effective in treating Gram-positive bacteremias and endocarditis caused by Gram-positive pathogens (including E. faecalis) other than S. aureus" (ibid., lines 6 to 9) but also that "the occasional adverse effects noted at a dose of 3 mg/kg every 12 hr seemed to preclude raising the dose further, and clinical trials were stopped" (ibid., lines 14 to 15). On page 430, penultimate paragraph, document D1 recapitulates that "daptomycin is a potent antibiotic that is bactericidal for all of the most important Gram-positive pathogens" and that "elevated doses of daptomycin suggested that it may cause muscle toxicity in some patients, and so the clinical trials were stopped".

37. Document D8, a press release, discloses that "Cubist Pharmaceutical Inc has initiated clinical trials for intravenous daptomycin" (abstract, lines 1 to 2). Daptomycin is said to have exhibited "a favourable side effect profile in clinical trials completed to date and will be administered as a once a day therapy" (ibid., lines 4 to 6). In a phase 3 trial patients "will receive 4 mg/kg intravenously once every 24 hours for 14 days" (ibid., lines 8 to 11) and in an open-label phase 2 trial "daptomycin dosage levels of 4 mg/kg and 6 mg/kg administered intravenously once every 24 hours will be compared to the 3 mg/kg every 12 hour regimen used in a previous Phase 2 study" (ibid., lines 11 to 15).

38. Thus, while document D1 reviews the results of completed clinical trials in humans which had shown that the treatment of bacterial infections with daptomycin was effective, document D8 does not report on the outcome of the clinical studies it describes.

39. Therefore, the board takes the view that document D1 represents the more promising springboard than document D8, and accepts that the clinical study reported in document D1, wherein 3 mg/kg daptomycin administered every 12 hours was used to treat bacterial infections, represents the closest state of the art for the purpose of the assessment of inventive step of the subject-matter of claim 1.

Technical problem and its solution

40. The subject-matter of claim 1 differs from the clinical study reported in document D1 in the combination of a dosing range of daptomycin, 3 to 10 mg/kg, with a particular dosing frequency, every 24 hours.

41. According to the appellant the technical effect associated with this difference is the treatment of bacterial infections in humans with an improvement in two aspects, efficacy at higher doses of daptomycin and avoidance of muscle toxicity. The appellant submitted that the problem to be solved could thus be formulated as the provision of an improved treatment for bacterial infections compared with the treatment disclosed in document D1, namely one that avoided muscle toxicity and was capable of showing increased efficacy at higher doses.

42. The respondents disputed that the problem to be solved could indeed be formulated as the provision of an improved treatment. First, an increased efficacy would be expected based on the prior art and could thus not be relied on for the formulation of the problem. Second, the patent provided data as regards the absence of adverse skeletal muscle effects in humans only for doses of 4 mg/kg and 6 mg/kg daptomycin administered every 24 hours, but not for higher doses of daptomycin.

43. The board considers that the respondents' argument as regards efficacy appears to go to obviousness ("would be expected"), but at the same time concedes that a dose of daptomycin that is higher than the 3 mg/kg of daptomycin disclosed in document D1 would indeed be expected to be more efficacious (see also point 36 above).

As to the respondents' argument concerning the lack of evidence for the absence of muscle toxicity over the whole range claimed, the board accepts that the dog studies (see examples 1 to 3) and the human studies (see example 4) reported in the patent together credibly show that administration of daptomycin every 24 hours minimises skeletal muscle toxicity. The board thus also accepts that the problem to be solved is as formulated by the appellant.

Obviousness

44. The question which remains to be answered is whether the skilled person, aware of the teaching of document D1 and faced with the technical problem, would have modified the teaching of the closest prior art document D1 so as to arrive at the claimed invention in an obvious manner.

45. One embodiment of the invention as claimed is the administration of daptomycin at a dosage regimen of 3 mg/kg once every 24 hours. It is this embodiment which will be considered in the following.

46. As set out above (see point 36), document D1 discloses that daptomycin's bactericidal effect is dose-dependent, that 2 mg/kg given every 24 hours is effective as is 3 mg/kg given every 12 hours but also that some patients experienced adverse effects at 3 mg/kg given every 12 hours and that clinical trials were stopped because results at elevated doses of daptomycin suggested that it may cause muscle toxicity in some patients.

47. In the board's view, the skilled person starting from a dosage regimen wherein 3 mg/kg daptomycin is administered every 12 hours and looking for a dosage regimen which while maintaining the efficacy of daptomycin reduces its toxicity (see the problem formulated in point 41 above) would have turned to document D13.

This document discloses that skeletal muscle has been identified as the target organ of daptomycin toxicity and reports on two studies conducted in dogs to investigate the potential effects of dose fractionation on toxicity. It reports that it has been found that toxicity was not related to the peak concentration of daptomycin that occurs in the bloodstream after administration (Cmax) or to the total concentration of daptomycin in the bloodstream for 24 hours (AUC24h) and that the data suggested that the dosing interval had a greater influence on toxicity than did the dose itself. It was hypothesised that once-daily administration of daptomycin would lead to lower toxicity because it would allow greater time between doses for repair of subclinical muscle damage associated with daptomycin.

Further it also discloses that studies in animal efficacy models have demonstrated that effectiveness of daptomycin is optimised by once-daily dosing since Cmax was found to be the key pharmacokinetic parameter associated with eradication of infection.

Document D13 concludes that the results suggested that once-daily dosing could minimise daptomycin muscle toxicity, while optimising its antimicrobial efficacy.

48. In the board's view, document D13 thus gives the skilled person a reasonable expectation that a once- daily dosing regimen of daptomycin is safe with respect to skeletal muscle toxicity, also in humans (see also point 55 below).

49. As set out above (see point 37), document D8 discloses that clinical trials have been initiated in which 4 or 6 mg/kg of daptomycin will be given once every 24 hours to patients. In the board's view, the disclosure of document D8 thus would reassure the skilled person that once-daily dosing of daptomycin in humans is the way forward.

50. As a first line of argument the appellant submitted that document D1 taught away from the invention by suggesting that higher, more frequent dosing was required for efficacy (see page 424, third full paragraph), but that this was not considered to be a realistic option because of the known side effects in muscle (see page 424, first full paragraph).

51. The appellant's argument implies that the skilled person would take from document D1 the suggestion of an alternative that he would consider so promising that he would abandon the teaching from the combination of documents D1 and D13. The board is not persuaded however that this is what the skilled person would do since document D1 itself also discloses that the suggested higher and more frequent dosing was not an option.

52. The appellant further submitted that document D1 proposed a solution different from the claimed one, namely the use of a daptomycin analog (see page 430, final paragraph).

53. The board notes that document D1 was published in 1997. The content of document D13 was thus not available at the time when document D1 was written. Thus it does not help the appellant's case that the author of document D1 - unaware of the teaching of document D13 - suggested other solutions, e.g. daptomycin analogs. At the effective date of the claim under consideration the skilled person was aware of the teaching of document D13 and would have considered that once-daily administration of daptomycin would avoid muscle toxicity (see point 47 above).

54. The appellant also disputed that the skilled person would even consider the teaching of document D13 as it reported on dog studies and not on human clinical trials. Furthermore, the skilled person would not separate the two aspects of the dosage regimen disclosed in document D13, i.e. once-daily dosing at a dose of 75 mg/kg daptomycin.

55. The board is not persuaded by these arguments either. As to the first argument, daptomycin has been developed for use in humans (see e.g. document D1, page 423, third paragraph, to page 424, fourth paragraph) and the skilled person reading document D13 is aware of this. Moreover, the kind of toxicity that is studied in document D13 is the one that is relevant to daptomycin's use in humans - this toxicity is already mentioned in document D1 (see page 430, third paragraph). It is thus, first, very unlikely that the authors of document D13 would have studied dogs unless the results thus obtained were relevant for humans. Second, when document D13 concludes that "once-daily" is safe, the skilled person understands that this statement applies primarily to humans, since to gain more insight into the use of daptomycin in humans was the whole point of the study in dogs. In this context the board considers that it would not have escaped the skilled person that the dog studies in document D13 were carried out by the same company that had initiated clinical trials in humans which involved once-daily administration of daptomycin, see document D8.

56. As to the second argument, document D13 makes it clear that different parameters are responsible for toxicity and efficacy of daptomycin. Thus, while muscle toxicity did not appear to be directly related to Cmax, Cmax was the key pharmacokinetic parameter associated with eradication of infection (see document D13, abstract). From document D1 the skilled person knows that a dose of 3 mg/kg daptomycin is effective in humans in treating Gram-positive bacteremias (see page 424, second paragraph). In the board's view, the skilled person would therefore not use the dose of 75 mg/kg daptomycin disclosed in document D13 for dogs but a dose of 3 mg/kg daptomycin.

57. The board concludes from the above that the skilled person would take once-daily administration from document D13 and apply it to the dose of daptomycin known to be efficacious in humans from document D1, 3 mg/kg, and thus arrive in an obvious manner at a dosage regimen, 3 mg/kg once every 24 hours, falling within the scope of claim 1. Consequently, the skilled person would have arrived at this embodiment of claim 1 in an obvious manner.

58. Therefore, the subject-matter of claim 1 as a whole must be considered to fail to meet the requirements of Article 56 EPC 1973.

New auxiliary request

Admission into the appeal proceedings

59. Claim 1 of the new auxiliary request differed from claim 1 of the main request in that the dose was now limited to 4 or 6 mg/kg of daptomycin (see section XII). The new auxiliary request amounted to an amendment to the appellant's case and its admission was thus at the board's discretion (Article 13 RPBA).

60. This claim request was filed on the second day of the oral proceedings after the board had given its opinion on inventive step of the subject-matter of claim 1 of the main request.

61. The appellant submitted that taking document D1 instead of document D8 as the closest prior art changed the inventive step analysis and that the combination of documents D1 and D13 had not been made prominently on appeal before. The mere back-reference in respondent I's reply to the statement of grounds of appeal to its earlier submissions as regards lack of inventive step was not sufficient under Article 12(2) RPBA. The new auxiliary request was a simple amendment in reaction to the board's opinion and should therefore be admitted into the appeal proceedings.

62. However, as already noted before, the opposition division had held that the subject-matter of claim 1 of the main request lacked inventive step over document D8 as the closest prior art in combination with the teaching of documents D13 and/or D1 (see point 32 above), i.e. the same three documents considered during these appeal proceedings in the context of inventive step right from the beginning.

63. Moreover, the line of reasoning starting from document D1 as closest prior art was the appellant's own case. And, as regards document D13, the respondents merely maintained that regardless of whether document D1 or document D8 was taken as the closest prior art, document D13 rendered once-daily administration of daptomycin obvious for the avoidance of muscle toxicity.

64. The board also considered that the line of argument relying on a combination of documents D1 and D13 could not be perceived as being hidden in the respondents' submissions or as being presented in a manner that it could be expected not to be taken into account by the board. Firstly, in the present case, the back-reference to submissions made during the proceedings before the opposition division was sufficient under Article 12(2) RPBA since (i) the relevant passages in the earlier submission were specifically identified, (ii) the line of argument was not contradicted by the decision of the opposition division, which was based on a different line of argumentation, and (iii) the subject-matter concerned was unchanged. Moreover, respondent II had mentioned the combination of documents D1 and D13 explicitly in its reply to the statement of grounds of appeal.

65. The board further noted that the appellant's main defense in relation to document D13 up to that point had been to argue that the document was not prior art.

66. In view of the above mentioned considerations the board concluded that there was no change in the case, certainly not one that qualified as an unforeseeable development in the proceedings. Moreover, that a board in inter partes proceedings finds at oral proceedings against a party is also not unexpected. Thus, filing of the amendment on the second day of the oral proceedings after the board had given its opinion on inventive step of the subject-matter of claim 1 of the main request could not be justified by the circumstances of the case.

67. And, furthermore, as regards the submission that the amendment was simple the board considers that, while the amendment as such might have been simple in the sense that it was easily understandable what the amendment was, in terms of lines of arguments to be considered, the consequences might not have been simple.

68. Finally, it was also not immediately apparent to the board that the new claim request was clearly and obviously allowable as document D8 already disclosed the administration of 4 or 6 mg/kg of daptomycin once daily in humans (see point 37).

69. Therefore, the board decided not to admit the new auxiliary request into the appeal proceedings (Article 13(1) and (3) RPBA).