WO1997000883A1 - Composes regulateurs de la meiose - Google Patents
Composes regulateurs de la meiose Download PDFInfo
- Publication number
- WO1997000883A1 WO1997000883A1 PCT/DK1996/000271 DK9600271W WO9700883A1 WO 1997000883 A1 WO1997000883 A1 WO 1997000883A1 DK 9600271 W DK9600271 W DK 9600271W WO 9700883 A1 WO9700883 A1 WO 9700883A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- meiosis
- compound
- general formula
- hydrogen
- compound according
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 49
- 230000021121 meiosis Effects 0.000 title claims abstract description 40
- 230000001105 regulatory effect Effects 0.000 title claims abstract description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 14
- 239000001257 hydrogen Substances 0.000 claims abstract description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
- 210000000287 oocyte Anatomy 0.000 claims description 13
- 210000004602 germ cell Anatomy 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 9
- 210000003794 male germ cell Anatomy 0.000 claims description 6
- 239000003814 drug Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 210000004027 cell Anatomy 0.000 claims description 3
- 241000124008 Mammalia Species 0.000 claims description 2
- 230000018046 regulation of meiosis Effects 0.000 claims description 2
- 239000000126 substance Substances 0.000 description 13
- 230000001939 inductive effect Effects 0.000 description 9
- 239000000203 mixture Substances 0.000 description 7
- 239000003433 contraceptive agent Substances 0.000 description 5
- RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229940124558 contraceptive agent Drugs 0.000 description 3
- 210000004420 female germ cell Anatomy 0.000 description 3
- 230000036512 infertility Effects 0.000 description 3
- 208000000509 infertility Diseases 0.000 description 3
- 231100000535 infertility Toxicity 0.000 description 3
- 238000003744 In vitro fertilisation Methods 0.000 description 2
- 229930182558 Sterol Natural products 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 210000000349 chromosome Anatomy 0.000 description 2
- 230000002254 contraceptive effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000262 estrogen Substances 0.000 description 2
- 229940011871 estrogen Drugs 0.000 description 2
- 230000001605 fetal effect Effects 0.000 description 2
- 230000003054 hormonal effect Effects 0.000 description 2
- FDGQSTZJBFJUBT-UHFFFAOYSA-N hypoxanthine Chemical compound O=C1NC=NC2=C1NC=N2 FDGQSTZJBFJUBT-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 230000027758 ovulation cycle Effects 0.000 description 2
- 210000004681 ovum Anatomy 0.000 description 2
- 239000008194 pharmaceutical composition Substances 0.000 description 2
- 229960003387 progesterone Drugs 0.000 description 2
- 239000000186 progesterone Substances 0.000 description 2
- 239000000583 progesterone congener Substances 0.000 description 2
- 230000031877 prophase Effects 0.000 description 2
- 230000033458 reproduction Effects 0.000 description 2
- 210000001082 somatic cell Anatomy 0.000 description 2
- 150000003432 sterols Chemical class 0.000 description 2
- 235000003702 sterols Nutrition 0.000 description 2
- 210000001550 testis Anatomy 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 108091028026 C-DNA Proteins 0.000 description 1
- 239000002126 C01EB10 - Adenosine Substances 0.000 description 1
- 241000557626 Corvus corax Species 0.000 description 1
- 108020004414 DNA Proteins 0.000 description 1
- 230000006820 DNA synthesis Effects 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 102000006771 Gonadotropins Human genes 0.000 description 1
- 108010086677 Gonadotropins Proteins 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- UGQMRVRMYYASKQ-UHFFFAOYSA-N Hypoxanthine nucleoside Natural products OC1C(O)C(CO)OC1N1C(NC=NC2=O)=C2N=C1 UGQMRVRMYYASKQ-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229960005305 adenosine Drugs 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 230000023752 cell cycle switching, mitotic to meiotic cell cycle Effects 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000035558 fertility Effects 0.000 description 1
- 230000003325 follicular Effects 0.000 description 1
- 210000001733 follicular fluid Anatomy 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 210000002149 gonad Anatomy 0.000 description 1
- 239000002622 gonadotropin Substances 0.000 description 1
- 229940094892 gonadotropins Drugs 0.000 description 1
- 210000002503 granulosa cell Anatomy 0.000 description 1
- 210000003313 haploid nucleated cell Anatomy 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000008774 maternal effect Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000005906 menstruation Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000007922 nasal spray Substances 0.000 description 1
- 229940097496 nasal spray Drugs 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 230000016087 ovulation Effects 0.000 description 1
- 230000000624 ovulatory effect Effects 0.000 description 1
- 230000008775 paternal effect Effects 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 210000004508 polar body Anatomy 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000035935 pregnancy Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003212 purines Chemical class 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 230000014639 sexual reproduction Effects 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
Definitions
- the present invention relates to pharmacologically active compounds and to their use as medicaments. More particularly it has been found that the compounds of the invention can be used for regulating the meiosis.
- Meiosis is the unique and ultimate event of germ cells on which sexual reproduction is based. Meiosis comprises two meiotic divisions. During the first division, exchange between maternal and paternal genes take place before the pairs of chromosomes are separated into the two daughter cells. These contain only half the number (1n) of chromosomes and 2c DNA. The second meiotic division proceeds without a DNA synthesis. This division therefore results in the formation of the haploid germ cells with only 1 c DNA.
- the meiotic events are similar in the male and female germ cells, but the time schedule and the differentiation processes which lead to ova and to spermatozoa differ profoundly.
- All female germ cells enter the prophase of the first meiotic division early in life, often before birth, but all are arrested as oocytes later in the prophase (dictyate state) until ovulation after puberty.
- the female has a stock of oocytes which is drawn upon until the stock is exhausted.
- Meiosis in females is not completed until after fertilisation, and results in only one ovum and two abortive polar bodies per germ cell.
- only some of the male germ cells enter meiosis from puberty and leave a stem population of germ cells throughout life. Once initiated, meiosis in the male cell proceeds without significant delay and produces four spermatozoa.
- MAS meiosis activating substance
- MPS meiosis preventing substance
- novel, stable compounds with interesting pharmacological properties.
- the compounds of the invention are useful for regulating the meiosis in oocytes and in male germ cells.
- R 1 , R 2 and R 3 independently, are hydrogen or methyl; R 4 and R 5 are either hydrogen or together they designate an additional bond between the carbon atoms to which they are bound.
- the present invention relates to a compound of the general formula (I) wherein R 1 is hydrogen.
- the present invention relates to a compound of the general formula (I) wherein R 1 is methyl.
- the present invention relates to a compound of the general formula (I) wherein R 2 is hydrogen.
- the present invention relates to a compound of the general formula (I) wherein R 2 is methyl.
- the present invention relates to a compound of the general formula (I) wherein R 3 is hydrogen.
- the present invention relates to a compound of the general formula (I) wherein R 3 is methyl.
- the present invention relates to a compound of the general formula (I) wherein R 4 and R5 are both hydrogen.
- the present invention relates to a compound of the general formula (I) wherein R 4 and R5 together designate an additional double bond between the carbon atoms to which they are bound.
- the present invention relates to the use of a compound of the general formula (I) in the manufacture of a medicament.
- the present invention relates to the use of a compound of the general formula (I) in the manufacture of a medicament for use in the regulation of meiosis.
- the expression "regulating the meiosis” is understood to indicate that the compounds can be used for stimulating the meiosis in vitro, in vivo, and ex vivo.
- the present invention relates to the use of a compound of the general formula (I) in the regulation of the meiosis of oocytes or male germ cells.
- the present invention relates to a method of regulating the meiosis in a mammalian germ cell which method comprises administering an effective amount of a compound of the general formula (I) above to a germ cell in need of such a treatment.
- the compounds of the present invention will induce resumption of meiosis in oocytes as well as in male germ cells.
- the existence of a meiosis inducing substance in nature has been known for some time. However, until recently the identity of the meiosis inducing substance or substances has been unknown.
- the compounds of the general formula (I) are used to stimulate the meiosis.
- the compounds of the general formula (I) are used to stimulate the meiosis in humans.
- the compounds of formula (I) are promising as new fertility regulating agents without the usual side effect on the somatic cells which are known from the hitherto used hormonal contraceptives which are based on estrogens and/or gestagens.
- a meiosis inducing substance can be administered so as to prematurely induce resumption of meiosis in oocytes while they are still in the growing follicle, before the ovulatory peak of gonadotropins occurs.
- the resumption of the meiosis can, for example, be induced a week after the preceding menstruation has ceased.
- the resulting overmature oocytes are then most likely not to be fertilised. The normal menstrual cycle is not likely to be affected.
- a meiosis inducing substance of the general formula (I) can be used in the treatment of certain cases of infertility in females, including women, by administration thereof to females who, due to an insufficient own production of MIS, are unable to produce mature oocytes. Also, when in vitro fertilisation is performed, better results can be achieved, when a meiosis inducing substance of the general formula (I) is added to the medium in which the oocytes are kept. Also, when infertility in males, including men, is caused by an insufficient own production of the meiosis inducing substance administration of a meiosis inducing substance of the general formula (I) can be used for relieving the problem.
- the route of administration of the compositions containing a compound of formula (I) may be any route which effectively transports the active compound to its site of action.
- compositions which comprises at least one compound of formula (I) in connection with a phar ⁇ maceutically acceptable carrier.
- a pharmaceutical composition which comprises at least one compound of formula (I) in connection with a phar ⁇ maceutically acceptable carrier.
- such compositions are preferably in the form of capsules or tablets.
- the pharmaceutical compositions may comprise carriers, diluents, abso ⁇ tion enhancers, preservatives, buffers, agents for adjusting the osmotic pressure, tablet disintegrating agents and other ingredients which are conventionally used in the art.
- solid carriers are magnesium carbonate, magnesium stearate, dextrin, lactose, sugar, talc, gelatine, pectin, tragacanth, methyl cellulose, sodium carboxymethyl cellulose, low melting waxes and cocoa butter.
- Liquid compositions include sterile solutions, suspensions and emulsions. Such liquid compositions may be suitable for injection or for use in connection with ex vivo and in vitro fertilisation.
- the liquid compositions may contain other ingredients which are conventionally used in the art, some of which are mentioned in the list above.
- composition for transdermal administration of a compound of this invention may be provided in the form of a patch and a composition for nasal administration may be provided in the form of a nasal spray in liquid or powder form.
- the dose of a compound of the invention to be used will be determined by a physician and will depend, inter alia, on the particular compound employed, on the route of administration and on the purpose of the use.
- the compounds of the general formula (I) can be synthesised by methods known per se.
- Examples of preferred compounds of the general formula (I) are the following:
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU61226/96A AU6122696A (en) | 1995-06-23 | 1996-06-20 | Meiosis regulating compounds |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK0729/95 | 1995-06-23 | ||
DK72995 | 1995-06-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997000883A1 true WO1997000883A1 (fr) | 1997-01-09 |
Family
ID=8096873
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/DK1996/000271 WO1997000883A1 (fr) | 1995-06-23 | 1996-06-20 | Composes regulateurs de la meiose |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU6122696A (fr) |
WO (1) | WO1997000883A1 (fr) |
ZA (1) | ZA965332B (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000050066A1 (fr) * | 1999-02-24 | 2000-08-31 | Novo Nordisk A/S | Traitement de l'infecondite |
WO2000050065A1 (fr) * | 1999-02-24 | 2000-08-31 | Novo Nordisk A/S | Traitement de l'infecondite |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996000235A1 (fr) * | 1994-06-23 | 1996-01-04 | Novo Nordisk A/S | Derives du type sterol utilises pour reguler la meiose |
-
1996
- 1996-06-20 WO PCT/DK1996/000271 patent/WO1997000883A1/fr active Application Filing
- 1996-06-20 AU AU61226/96A patent/AU6122696A/en not_active Abandoned
- 1996-06-24 ZA ZA965332A patent/ZA965332B/xx unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996000235A1 (fr) * | 1994-06-23 | 1996-01-04 | Novo Nordisk A/S | Derives du type sterol utilises pour reguler la meiose |
Non-Patent Citations (1)
Title |
---|
J. CHEM. SOC. PERKIN TRANS., Volume 1, 1983, MARIO ANASTASIA, "A New Route to Steroid Ring-c Aromatization from 7-Oxygenated Steroids", page 587 - page 590. * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000050066A1 (fr) * | 1999-02-24 | 2000-08-31 | Novo Nordisk A/S | Traitement de l'infecondite |
WO2000050065A1 (fr) * | 1999-02-24 | 2000-08-31 | Novo Nordisk A/S | Traitement de l'infecondite |
US6281013B1 (en) * | 1999-02-24 | 2001-08-28 | Novo Nordisk A/S | Treatment of Infertility |
US6585982B1 (en) | 1999-02-24 | 2003-07-01 | Nna/S | Treatment of infertility |
Also Published As
Publication number | Publication date |
---|---|
ZA965332B (en) | 1997-01-23 |
AU6122696A (en) | 1997-01-22 |
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