Wednesday, July 8, 2026

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Grace Therapeutics

Grace Therapeutics drug portfolio — 37 indexed compounds with therapeutic class and molecular targets from public FDA and regional approval metadata.

3009, boul. de la Concorde E., Suite 102, Laval, Québec H7E 2B5, CA HQ
18 Employees
Public company Type
GRCE · NYSE Ticker
Company details
Status
Public
HQ
3009, boul. de la Concorde E., Suite 102, Laval, Québec H7E 2B5, CA
Employees
18
Programs
29
Drugs
37
Patents
34
Intelligence · Drug Pipeline

Grace Therapeutics pipeline

Portfolio lens on 37 drugs and development assets — regulatory status, targets, and deep links to NovaPharmaNews drug profiles.

Grace Therapeutics drug portfolio — 37 indexed compounds with therapeutic class and molecular targets from public FDA and regional approval metadata.

Drug portfolio

37 compounds
  1. US regulatory status: approved. Molecular target: Tyrosine-protein kinase BTK.

    Target
    Tyrosine-protein kinase BTK
    Mechanism
    Tyrosine-protein kinase BTK inhibitor
  2. Development asset linked to Grace Therapeutics in public FDA and regional records.

  3. Development asset linked to Grace Therapeutics in public FDA and regional records.

  4. US regulatory status: approved. Molecular target: Cyclooxygenase.

    Target
    Cyclooxygenase
    Mechanism
    Cyclooxygenase inhibitor
  5. benralizumab

    Respiratory system (R03)

    US regulatory status: approved. Molecular target: Interleukin-5 receptor subunit alpha.

    Target
    Interleukin-5 receptor subunit alpha
    Mechanism
    Interleukin-5 receptor subunit alpha inhibitor
  6. bupivacaine

    Nervous system (N01)

    US regulatory status: approved. Molecular target: Sodium channel protein type 4 subunit alpha.

    Target
    Sodium channel protein type 4 subunit alpha
    Mechanism
    Sodium channel protein type IV alpha subunit blocker
  7. US regulatory status: approved. Mechanism: Dihydrofolate reductase inhibitor.

    Mechanism
    Dihydrofolate reductase inhibitor
  8. US regulatory status: approved. Molecular target: 70S ribosome.

    Target
    70S ribosome
    Mechanism
    70S ribosome inhibitor
  9. US regulatory status: approved. Molecular target: Aromatic-L-amino-acid decarboxylase.

    Target
    Aromatic-L-amino-acid decarboxylase
    Mechanism
    DOPA decarboxylase inhibitor
  10. US regulatory status: approved. Mechanism: Unknown.

    Mechanism
    Unknown
  11. US regulatory status: approved. Molecular target: Adrenergic receptor alpha-2.

    Target
    Adrenergic receptor alpha-2
    Mechanism
    Adrenergic receptor alpha-2 agonist
  12. Development asset linked to Grace Therapeutics in public FDA and regional records.

  13. US regulatory status: approved. Molecular target: Sodium-dependent noradrenaline transporter.

    Target
    Sodium-dependent noradrenaline transporter
    Mechanism
    Norepinephrine transporter inhibitor
  14. US regulatory status: approved. Molecular target: Sodium-dependent noradrenaline transporter.

    Target
    Sodium-dependent noradrenaline transporter
    Mechanism
    Norepinephrine transporter inhibitor
  15. US regulatory status: approved. Molecular target: Sodium-dependent noradrenaline transporter.

    Target
    Sodium-dependent noradrenaline transporter
    Mechanism
    Serotonin transporter inhibitor
  16. Development asset linked to Grace Therapeutics in public FDA and regional records.

  17. US regulatory status: approved. Molecular target: Glutamate [NMDA] receptor.

    Target
    Glutamate [NMDA] receptor
    Mechanism
    Glutamate [NMDA] receptor negative allosteric modulator
  18. US regulatory status: approved. Molecular target: Mu-type opioid receptor.

    Target
    Mu-type opioid receptor
    Mechanism
    Mu opioid receptor agonist
  19. US regulatory status: approved. Mechanism: Supplement.

    Mechanism
    Supplement
  20. Development asset linked to Grace Therapeutics in public FDA and regional records.

  21. Development asset linked to Grace Therapeutics in public FDA and regional records. Mechanism: Mu opioid receptor agonist.

    Mechanism
    Mu opioid receptor agonist
  22. US regulatory status: approved. Molecular target: Mu-type opioid receptor.

    Target
    Mu-type opioid receptor
    Mechanism
    Mu opioid receptor agonist
  23. imiquimod

    Dermatologicals (D06)

    US regulatory status: approved. Molecular target: Toll-like receptor 7.

    Target
    Toll-like receptor 7
    Mechanism
    Toll-like receptor 7 agonist
  24. US regulatory status: approved. Molecular target: Glutamate [NMDA] receptor.

    Target
    Glutamate [NMDA] receptor
    Mechanism
    Glutamate [NMDA] receptor negative allosteric modulator
  25. Development asset linked to Grace Therapeutics in public FDA and regional records.

  26. US regulatory status: approved. Mechanism: Adrenergic receptor alpha agonist.

    Mechanism
    Adrenergic receptor alpha agonist
  27. Development asset linked to Grace Therapeutics in public FDA and regional records.

  28. US regulatory status: approved. Molecular target: GABA-A receptor; anion channel.

    Target
    GABA-A receptor; anion channel
    Mechanism
    GABA-A receptor; anion channel positive allosteric modulator
  29. Development asset linked to Grace Therapeutics in public FDA and regional records.

  30. tirzepatide

    Alimentary tract and metabolism (A10)

    US regulatory status: approved. Molecular target: Gastric inhibitory polypeptide receptor.

    Target
    Gastric inhibitory polypeptide receptor
    Mechanism
    Glucagon-like peptide 1 receptor agonist
  31. Development asset linked to Grace Therapeutics in public FDA and regional records.

  32. Development asset linked to Grace Therapeutics in public FDA and regional records. Mechanism: Norepinephrine transporter inhibitor.

    Mechanism
    Norepinephrine transporter inhibitor
  33. zinc

    Alimentary tract and metabolism (A16)

    Alimentary tract and metabolism (A16) compound in Grace Therapeutics's portfolio. Mechanism: Blocks absorption of copper and induces the production of the copper-binding protein metallothionein..

    Mechanism
    Blocks absorption of copper and induces the production of the copper-binding protein metallothionein.