Finasteride/latanoprost/minoxidil (developmental code name TH-07 or TH07) is a topical combination drug which is under development for the treatment of alopecia (hair loss).[1][2][3] It is specifically a combination of finasteride (Propecia) (0.1%), a 5α-reductase inhibitor (5α-RI); latanoprost (Xalatan) (0.03%), a prostaglandin F2α analogue and prostaglandin F receptor agonist; and minoxidil (Rogaine) (5%), a KATP potassium channel opener.[1] All three of these drugs have individually been shown to stimulate hair growth in the setting of alopecia, and both finasteride and minoxidil are approved and widely used for treatment of alopecia.[4][5][6][7] Finasteride/latanoprost/minoxidil is under development by Triple Hair.[1][2] As of December 2023, the drug is in phase 2 clinical trials.[1]
See also
References
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Androgens (incl. AASTooltip anabolic–androgenic steroid) | |
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| Antiandrogens | | ARTooltip Androgen receptor antagonists | |
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Steroidogenesis inhibitors | |
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| Antigonadotropins |
- D2 receptor antagonists (prolactin releasers) (e.g., domperidone, metoclopramide, risperidone, haloperidol, chlorpromazine, sulpiride)
- Estrogens (e.g., bifluranol, diethylstilbestrol, estradiol, estradiol esters, ethinylestradiol, ethinylestradiol sulfonate, paroxypropione)
- GnRH agonists (e.g., leuprorelin)
- GnRH antagonists (e.g., cetrorelix)
- Progestogens (incl., chlormadinone acetate, cyproterone acetate, hydroxyprogesterone caproate, gestonorone caproate, medroxyprogesterone acetate, megestrol acetate)
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| Others | |
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Receptor (ligands) | | DP (D2)Tooltip Prostaglandin D2 receptor | | DP1Tooltip Prostaglandin D2 receptor 1 | |
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| DP2Tooltip Prostaglandin D2 receptor 2 | |
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| EP (E2)Tooltip Prostaglandin E2 receptor | | EP1Tooltip Prostaglandin EP1 receptor |
- Antagonists: AH-6809
- ONO-8130
- SC-19220
- SC-51089
- SC-51322
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| EP2Tooltip Prostaglandin EP2 receptor |
- Antagonists: AH-6809
- PF-04418948
- TG 4-155
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| EP3Tooltip Prostaglandin EP3 receptor | |
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| EP4Tooltip Prostaglandin EP4 receptor |
- Antagonists: Grapiprant
- GW-627368
- L-161982
- ONO-AE3-208
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| Unsorted | |
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| FP (F2α)Tooltip Prostaglandin F receptor | |
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| IP (I2)Tooltip Prostacyclin receptor | |
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| TP (TXA2)Tooltip Thromboxane receptor | |
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| Unsorted |
- Arbaprostil
- Ataprost
- Ciprostene
- Clinprost
- Cobiprostone
- Delprostenate
- Deprostil
- Dimoxaprost
- Doxaprost
- Ecraprost
- Eganoprost
- Enisoprost
- Eptaloprost
- Esuberaprost
- Etiproston
- Fenprostalene
- Flunoprost
- Froxiprost
- Lanproston
- Limaprost
- Luprostiol
- Meteneprost
- Mexiprostil
- Naxaprostene
- Nileprost
- Nocloprost
- Ornoprostil
- Oxoprostol
- Penprostene
- Pimilprost
- Piriprost
- Posaraprost
- Prostalene
- Rioprostil
- Rivenprost
- Rosaprostol
- Spiriprostil
- Tiaprost
- Tilsuprost
- Tiprostanide
- Trimoprostil
- Viprostol
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Enzyme (inhibitors) | COX (PTGS) | |
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| PGD2STooltip Prostaglandin D synthase | |
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| PGESTooltip Prostaglandin E synthase | HQL-79 |
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| PGFSTooltip Prostaglandin F synthase | |
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| PGI2STooltip Prostacyclin synthase | |
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| TXASTooltip Thromboxane A synthase | |
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| Others | |
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- See also
- Receptor/signaling modulators
- Leukotriene signaling modulators
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| Calcium | | VDCCsTooltip Voltage-dependent calcium channels | |
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| Potassium | | VGKCsTooltip Voltage-gated potassium channels | |
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| IRKsTooltip Inwardly rectifying potassium channel | | Blockers | |
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| Activators |
- GIRKTooltip G protein-coupled inwardly rectifying potassium channel-specific: ML-297 (VU0456810)
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| KCaTooltip Calcium-activated potassium channel | |
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| K2PsTooltip Tandem pore domain potassium channel | |
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| Sodium | | VGSCsTooltip Voltage-gated sodium channels | |
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| ENaCTooltip Epithelial sodium channel | |
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| ASICsTooltip Acid-sensing ion channel | |
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| Chloride | | CaCCsTooltip Calcium-activated chloride channel | |
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| CFTRTooltip Cystic fibrosis transmembrane conductance regulator | |
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| Unsorted | |
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| Others | | TRPsTooltip Transient receptor potential channels | |
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| LGICsTooltip Ligand gated ion channels | |
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See also: Receptor/signaling modulators • Transient receptor potential channel modulators |