Therapeutic use of diaminophenothiazines

1. A method of treatment of a cognitive or CNS disorder in a patient, wherein said disorder is one which is susceptible to treatment by a 3,7-diaminophenothiazine (DAPTZ) compound,

which method comprises orally administering to said patient a dosage unit containing at least 50 mg of said DAPTZ compound in stable crystalline reduced form as active ingredient,

wherein said DAPTZ compound is selected from compounds of the following formula

wherein:

each of R 1 and R 9 is independently selected from: —H;

each of R 3NA and R 3NB is independently selected from: —H, C 1-4 alkyl, C 2-4 alkenyl, and halogenated C 1-4 alkyl;

each of R 7NA and R 7NB is independently selected from: —H, C 1-4 alkyl, C 2-4 alkenyl, and halogenated C 1-4 alkyl;

each of HX 1 and HX 2 is independently a protic acid, wherein if any of HX 1 and HX 2 are hydrohalic acids, then each are independently selected from HCI or HBr; and

wherein the patient has a haematological disorder selected from a haemoglobinopathy, an anemia, a haematological malignancy, and a coagulopathy.

2. The method of claim 1 wherein the cognitive or CNS disorder is a tauopathy and wherein the treatment of the tauopathy is such that the DAPTZ compound causes inhibition of the aggregation of the tau protein associated with said disease state and also dissolution of tau aggregates in the brain of the patient or subject.

3. The method of claim 2 wherein the cognitive or CNS disorder is selected from the list consisting of: Alzheimer's disease, Pick's disease, progressive supranuclear palsy (PSP), fronto-temporal dementia with parkinsonism linked to chromosome 17, disinhibition-dementia-parkinsonism-amyotrophy complex, pallido-ponto-nigral degeneration, Guam-ALS syndrome; pallido-nigro-luysian degeneration, cortico-basal degeneration and mild cognitive impairment; Down's syndrome; postencephalitic parkinsonism; and parkinsonism with dementia complex of Guam.

4. The method of claim 1 wherein the cognitive or CNS disorder is a synucleinopathy, which is selected from the list consisting of: Parkinson's Disease, dementia with Lewy bodies, multiple system atrophy, drug-induced parkinsonism, and pure autonomic failure (PAF).

5. The method of claim 1 wherein the haematological disorder is selected from sickle-cell disease, thalassemia, methaemoglobinemia; haemolytic anemia; lymphoma, myeloma, plasmacytoma, leukemia, and hemophilia.

6. The method of claim 1 wherein the dosage unit is provided as a pharmaceutical composition comprising the DAPTZ compound and a pharmaceutically acceptable carrier, diluent, or excipient.

7. The method of claim 1 wherein the pharmaceutical composition is for a combination therapy and comprises in addition to the DAPTZ compound a further active ingredient selected from: a cholinesterase inhibitor; an NMDA receptor antagonist; a muscarinic receptor agonist; and an inhibitor of conversion of amyloid precursor protein to beta-amyloid.

8. The method of claim 1 wherein each of HX 1 and HX 2 is an organic acid.

9. The method of claim 8 wherein each of HX 1 and HX 2 is independently selected from H 2 CO 3 and CH 3 COOH.

10. The method of claim 1 wherein:

each of R 1 and R 9 is —H;

each of R 3NA and R 3NB is -Me;

each of R 7NA and R7NB is -Me;

each of HX 1 and HX 2 is independently a monoprotic acid.

11. The method of claim 6 wherein the composition is a tablet or capsule.

12. The method of claim 1 wherein the cognitive or CNS disorder is selected from:

CJD, nvCJD, fatal familial insomnia, Gerstmann-Straussler-Scheinker syndrome or Kuru where the protein is prion protein;

Huntington's disease where the protein is huntingtin;

Spinocerebellar ataxia 1, 2, 3, or 7 where the protein is ataxin 1, 2, 3 or 7;

Dentatorubropallidoluysian atrophy where the protein is atrophin;

Spinal and bulbar muscular atrophy where the protein is androgen receptor;

Familial encephalopathy with neuronal inclusion bodies where the protein is neuroserpin;

Hereditary cerebral angiopathy (Icelandic) where the protein is cystatin C; and

Amyotrophic lateral sclerosis where the protein is superoxide dismutase 1.