HRP20220837T1 - Terapeutski pripravci koji sadrže deuterirane ili djelomično deuterirane n,n-dimetiltriptaminske spojeve - Google Patents

Terapeutski pripravci koji sadrže deuterirane ili djelomično deuterirane n,n-dimetiltriptaminske spojeve Download PDF

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Publication number
HRP20220837T1
HRP20220837T1 HRP20220837TT HRP20220837T HRP20220837T1 HR P20220837 T1 HRP20220837 T1 HR P20220837T1 HR P20220837T T HRP20220837T T HR P20220837TT HR P20220837 T HRP20220837 T HR P20220837T HR P20220837 T1 HRP20220837 T1 HR P20220837T1
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HR
Croatia
Prior art keywords
dimethyltryptamine
pharmaceutically acceptable
prothio
dideutero
deutero
Prior art date
Application number
HRP20220837TT
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English (en)
Inventor
Peter RANDS
Zelah JOEL
Tiffanie BENWAY
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Small Pharma Ltd
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Publication of HRP20220837T1 publication Critical patent/HRP20220837T1/hr
Publication of HRP20220837T8 publication Critical patent/HRP20220837T8/hr

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/4045Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/14Radicals substituted by nitrogen atoms, not forming part of a nitro radical
    • C07D209/16Tryptamines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05Isotopically modified compounds, e.g. labelled

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Addiction (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Claims (14)

1. Pripravak koji sadrži: (a) α,α-dideutero-N,N-dimetiltriptaminski spoj, ili njegovu farmaceutski prihvatljivu sol; (b) α-protio, α-deutero-N,N-dimetiltriptaminski spoj, ili njegova farmaceutski prihvatljiva sol; i (c) N,N-dimetiltriptamin, ili njegove farmaceutski prihvatljive soli; pri čemu pripravak sadrži 50% ili više po težini spoja α,α-dideutero-N,N-dimetiltriptamina, ili njegove farmaceutski prihvatljive soli, i α-protio, α-deutero-N,N-dimetiltriptaminskog spoja, ili njegove farmaceutski prihvatljive soli.
2. Pripravak prema zahtjevu 1, koji se uglavnom sastoji od: a) α,α-dideutero-N,N-dimetiltriptamin, ili njegove farmaceutski prihvatljive soli; (b) α-protio, α-deutero-N,N-dimetiltriptamin, ili njegove farmaceutski prihvatljive soli; i (c) N,N-dimetiltriptamin, ili njegove farmaceutski prihvatljive soli; pri čemu je srednja molekularna težina α-protio, α-deutero-N,N-dimetiltriptamina, α,α-dideutero-N,N-dimetiltriptamina i N,N-dimetiltriptamina, prisutnih u pripravku od 188.90 do 190.28.
3. Pripravak prema zahtjevu 1 ili zahtjevu 2 sadrži 60% ili više po težini α,α-dideutero-N,N-dimetiltriptaminskog spoja, ili njegove farmaceutski prihvatljive soli, i α-protio, α-deutero-N,N -dimetiltriptaminski spoj, ili njegove farmaceutski prihvatljiva soli.
4. Pripravak prema bilo kojem od zahtjeva 1 do 3 naznačen time što je α,α-dideutero-N,N-dimetiltriptaminski spoj α,α-dideutero-N,N-dimetiltriptamin, ili njegova farmaceutski prihvatljiva sol.
5. Pripravak prema bilo kojem od zahtjeva 1, 3 i 4 sadrži α-protio, α-deutero-N,N-dimetiltriptaminski spoj odabran iz skupine koju čine α,β,β-trideutero-N,N-dimetiltriptamin, α,β-dideutero-N,N-dimetiltriptamin, i α-protio, α-deutero-N,N-dimetiltriptamin, i njihove farmaceutski prihvatljive soli.
6. Pripravak prema bilo kojem od zahtjeva 1 do 5 sadrži α-protio, α-deutero-N,N-dimetiltriptamin, ili njegovu farmaceutski prihvatljivu sol.
7. Pripravak prema bilo kojem od zahtjeva 1 do 6 koji ima čistoću veću ili jednaku 99% prema HPLC, poželjno čistoću veću ili jednaku 99.9% prema HPLC.
8. Pripravak prema bilo kojem od zahtjeva 1 do 7, naznačen time što su α-protio, α-deutero-N,N-dimetiltriptamin i α,α-dideutero-N,N-dimetiltriptamin spojevi, i N,N-dimetiltriptamin, u obliku farmaceutski prihvatljive soli, poželjno gdje je farmaceutski prihvatljiva sol fumaratna sol.
9. Pripravak prema bilo kojem od zahtjeva 1 do 7, naznačen time što su α-protio, α-deutero-N,N-dimetiltriptamin i α,α-dideutero-N,N-dimetiltriptamin spojevi, i N,N-dimetiltriptamin, u obliku fumaratne soli.
10. Pripravak kako je definiran u bilo kojem od zahtjeva 1 do 9 za uporabu u terapiji.
11. Pripravak kako je definiran u bilo kojem od zahtjeva 1 do 9 za uporabu u liječenju psihokognitivnog poremećaja kod pacijenata.
12. Pripravak za uporabu prema zahtjevu 11 naznačen time što je psihokognitivni poremećaj odabran iz skupine koja se sastoji od (i) opsesivno kompulzivnog poremećaja, (ii) depresivnog poremećaja, (iii) anksioznog poremećaja, (iv) zlouporabe tvari, i (v) poremećaja volje.
13. Pripravak za uporabu prema zahtjevu 12, naznačen time što je poremećaj veliki depresivni poremećaj, poželjno je da je poremećaj depresija otporna na liječenje.
14. Pripravak kako je definiran u bilo kojem od zahtjeva 1 do 9, za uporabu u psihoterapiji potpomognutoj dimetiltriptaminom.
HRP20220837TT 2019-06-03 2020-06-02 Terapeutski pripravci koji sadrže deuterirane ili djelomično deuterirane n,n-dimetiltriptaminske spojeve HRP20220837T8 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1907871.6A GB201907871D0 (en) 2019-06-03 2019-06-03 Therapeutic compositions
PCT/EP2020/065244 WO2020245133A1 (en) 2019-06-03 2020-06-02 Therapeutic compositions comprising deuterated or partially deuterated n,n-dimethyltryptamine compounds
EP20731372.7A EP3826632B1 (en) 2019-06-03 2020-06-02 Therapeutic compositions comprising deuterated or partially deuterated n,n-dimethyltryptamine compounds

Publications (2)

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HRP20220837T1 true HRP20220837T1 (hr) 2022-10-14
HRP20220837T8 HRP20220837T8 (hr) 2023-02-03

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US (2) US20220168275A1 (hr)
EP (2) EP4062910A1 (hr)
JP (1) JP2022535093A (hr)
KR (1) KR20220034061A (hr)
CN (1) CN114096246A (hr)
AU (1) AU2020286709B2 (hr)
BR (1) BR112021024333A2 (hr)
CA (2) CA3142290A1 (hr)
DK (1) DK3826632T3 (hr)
EA (1) EA202193338A1 (hr)
ES (1) ES2922101T3 (hr)
GB (4) GB201907871D0 (hr)
HR (1) HRP20220837T8 (hr)
HU (1) HUE059439T2 (hr)
IL (1) IL288617A (hr)
MX (1) MX2021014728A (hr)
PL (1) PL3826632T3 (hr)
PT (1) PT3826632T (hr)
TW (1) TW202210075A (hr)
WO (1) WO2020245133A1 (hr)

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US20220168275A1 (en) 2022-06-02
KR20220034061A (ko) 2022-03-17
GB2585978B (en) 2021-07-14
EP3826632B1 (en) 2022-05-18
GB2592822B (en) 2023-07-05
EP3826632A1 (en) 2021-06-02
GB2592822A (en) 2021-09-08
TW202210075A (zh) 2022-03-16
IL288617A (en) 2022-02-01
HUE059439T2 (hu) 2022-11-28
PL3826632T3 (pl) 2022-08-01
HRP20220837T8 (hr) 2023-02-03
EP4062910A1 (en) 2022-09-28
BR112021024333A2 (pt) 2022-02-08
CA3104072A1 (en) 2021-06-28
GB202100807D0 (en) 2021-03-10
US11771681B2 (en) 2023-10-03
DK3826632T3 (da) 2022-07-11
PT3826632T (pt) 2022-07-11
JP2022535093A (ja) 2022-08-04
GB2586940B (en) 2023-07-05
GB2586940A (en) 2021-03-10
AU2020286709A1 (en) 2022-01-06
CA3142290A1 (en) 2020-12-10
GB202107702D0 (en) 2021-07-14
GB202008303D0 (en) 2020-07-15
CN114096246A (zh) 2022-02-25
CA3104072C (en) 2022-07-19
GB2585978A (en) 2021-01-27
MX2021014728A (es) 2022-03-11
EA202193338A1 (ru) 2022-03-02
AU2020286709B2 (en) 2024-05-09
US20200390746A1 (en) 2020-12-17
ES2922101T3 (es) 2022-09-08
GB201907871D0 (en) 2019-07-17
WO2020245133A1 (en) 2020-12-10

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