Hereditary spastic paraplegia
MONDO:0019064Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs.
Also known as: spastic paraplegia, HSP, SPG, Strümpell-Lorrain disease, familial spastic paraplegia, hereditary spastic paraparesis, FSP, familial spastic paraparesis
33 clinical trials for this condition and its sub-types, 27 tagged with Hereditary spastic paraplegia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
Sub-types of Hereditary spastic paraplegia
-
Complex hereditary spastic paraplegia 1 trial · 7 incl. sub-types
50 sub-types
- Spastic paraplegia, optic atropy, and neuropathy 3 trials
- Hereditary spastic paraplegia 11 1 trial
- Hereditary spastic paraplegia 15 1 trial
- Hereditary spastic paraplegia 26 1 trial
- Hereditary spastic paraplegia 63 1 trial
- MASA syndrome 0 trials
- Troyer syndrome 0 trials
- Autosomal dominant complex spastic paraplegia 0 trials Sub-types →
- Autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction 0 trials
- Autosomal recessive complex spastic paraplegia type 9B 0 trials
- Autosomal recessive spastic paraplegia type 59 0 trials
- Autosomal recessive spastic paraplegia type 60 0 trials
- Autosomal recessive spastic paraplegia type 66 0 trials
- Autosomal recessive spastic paraplegia type 67 0 trials
- Autosomal recessive spastic paraplegia type 68 0 trials
- Autosomal recessive spastic paraplegia type 69 0 trials
- Autosomal recessive spastic paraplegia type 70 0 trials
- Autosomal recessive spastic paraplegia type 76 0 trials
- Autosomal recessive spastic paraplegia type 78 0 trials
- Fatty acid hydroxylase-associated neurodegeneration 0 trials
- Glutamate pyruvate transaminase 2 deficiency 0 trials
- Hereditary sensory and autonomic neuropathy with spastic paraplegia 0 trials
- Hereditary spastic paraplegia 18 0 trials Sub-types →
- Hereditary spastic paraplegia 23 0 trials
- Hereditary spastic paraplegia 24 0 trials
- Hereditary spastic paraplegia 25 0 trials
- Hereditary spastic paraplegia 27 0 trials
- Hereditary spastic paraplegia 32 0 trials
- Hereditary spastic paraplegia 39 0 trials Sub-types →
- Hereditary spastic paraplegia 43 0 trials
- Hereditary spastic paraplegia 44 0 trials
- Hereditary spastic paraplegia 45 0 trials
- Hereditary spastic paraplegia 46 0 trials
- Hereditary spastic paraplegia 49 0 trials
- Hereditary spastic paraplegia 53 0 trials
- Hereditary spastic paraplegia 54 0 trials
- Hereditary spastic paraplegia 55 0 trials
- Hereditary spastic paraplegia 57 0 trials
- Hereditary spastic paraplegia 61 0 trials
- Hereditary spastic paraplegia 64 0 trials
- Hereditary spastic paraplegia 74 0 trials
- Hereditary spastic paraplegia 75 0 trials
- Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome 0 trials
- Maternally-inherited spastic paraplegia 0 trials
- Spastic ataxia 2 0 trials
- Spastic paraplegia 84, autosomal recessive 0 trials
- Spastic paraplegia 85, autosomal recessive 0 trials
- Spastic paraplegia 86, autosomal recessive 0 trials
- Spastic paraplegia-glaucoma-intellectual disability syndrome 0 trials
- Spastic paraplegia-severe developmental delay-epilepsy syndrome 0 trials
-
Hereditary spastic paraplegia 50 3 trials
-
Hereditary spastic paraplegia 3A 2 trials
-
Hereditary spastic paraplegia 4 2 trials
-
Hereditary spastic paraplegia 5A 2 trials
-
Hereditary spastic paraplegia 47 1 trial
-
Hereditary spastic paraplegia 51 1 trial
-
Hereditary spastic paraplegia 52 1 trial
-
Hereditary spastic paraplegia 7 1 trial
-
Charcot-Marie-Tooth disease type 5 0 trials
-
Hereditary spastic paraplegia 10 0 trials
-
Hereditary spastic paraplegia 13 0 trials
-
Hereditary spastic paraplegia 14 0 trials
-
Hereditary spastic paraplegia 16 0 trials
-
Hereditary spastic paraplegia 2 0 trials
-
Hereditary spastic paraplegia 30 0 trials
2 sub-types
-
Hereditary spastic paraplegia 31 0 trials
-
Hereditary spastic paraplegia 33 0 trials
-
Hereditary spastic paraplegia 35 0 trials
-
Hereditary spastic paraplegia 48 0 trials
-
Hereditary spastic paraplegia 56 0 trials
-
Hereditary spastic paraplegia 6 0 trials
-
Hereditary spastic paraplegia 77 0 trials
-
Mast syndrome 0 trials
-
Pure hereditary spastic paraplegia 0 trials
12 sub-types
- Autosomal recessive spastic paraplegia type 71 0 trials
- Hereditary spastic paraplegia 12 0 trials
- Hereditary spastic paraplegia 19 0 trials
- Hereditary spastic paraplegia 28 0 trials
- Hereditary spastic paraplegia 34 0 trials
- Hereditary spastic paraplegia 37 0 trials
- Hereditary spastic paraplegia 41 0 trials
- Hereditary spastic paraplegia 42 0 trials
- Hereditary spastic paraplegia 62 0 trials
- Hereditary spastic paraplegia 72 0 trials
- Hereditary spastic paraplegia 73 0 trials
- Hereditary spastic paraplegia 8 0 trials
Most studied deeper sub-types
-
Halted gene therapy study raises questions for AMN patients
Disease control Stopped earlyThis early-stage trial tested a gene therapy called SBT101 for adrenomyeloneuropathy (AMN), a rare nerve disease that causes walking difficulties. Eight adults received either the therapy or a sham procedure. The study was terminated early, so we have limited data on safety and e…
Phase 1/2 • Sponsor: SwanBio Therapeutics, Inc. • Aim: Disease control
Last updated Aug 28, 2026 00:00 UTC
-
Rare disease mystery: scientists watch AMN progress in hopes of finding a cure
Knowledge-focused Stopped earlyThis study followed 65 adult men with a rare inherited nerve disease called AMN (a form of spastic paraplegia) to understand how their symptoms change over time. Researchers collected data on walking ability and quality of life. The goal was to fill gaps in knowledge about the di…
Sponsor: SwanBio Therapeutics, Inc. • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:56 UTC