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ARQ 092 is being investigated for patients with overgrowth diseases and/or vascular anomalies with genetic alterations of the PI3K/AKT pathway and may be available for patients who are ineligible for an ongoing ARQ 092 clinical trial or have other considerations that prevent access to ARQ 092 through an existing clinical trial.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ARQ 092 | Drug | Open-label expanded access for ARQ 092 capsules |
Inclusion Criteria:
Exclusion Criteria:
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| ID | Term |
|---|---|
| D016715 | Proteus Syndrome |
| D006130 | Growth Disorders |
| D009477 | Hereditary Sensory and Autonomic Neuropathies |
| D000013 | Congenital Abnormalities |
| ID | Term |
|---|---|
| D006223 | Hamartoma Syndrome, Multiple |
| D006222 | Hamartoma |
| D009369 | Neoplasms |
| D009378 | Neoplasms, Multiple Primary |
| D001848 | Bone Diseases, Developmental |
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
| D017880 | Limb Deformities, Congenital |
| D009139 | Musculoskeletal Abnormalities |
| D000015 | Abnormalities, Multiple |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009421 | Nervous System Malformations |
| D009422 | Nervous System Diseases |
| D020271 | Heredodegenerative Disorders, Nervous System |
| D019636 | Neurodegenerative Diseases |
| D011115 | Polyneuropathies |
| D010523 | Peripheral Nervous System Diseases |
| D009468 | Neuromuscular Diseases |
| D030342 | Genetic Diseases, Inborn |
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| ID | Term |
|---|---|
| C000608559 | Miransertib |
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