Telehealth clinic Shed announced on Tuesday that it has introduced Low-Dose Naltrexone (LDN), a therapeutic solution for individuals managing chronic pain, autoimmune diseases and metabolic health challenges.
The company said that LDN works by naturally balancing the immune system, reducing inflammation and providing pain relief, offering an alternative for patients seeking to address the root causes of their conditions.
LDN is a medication that temporarily blocks opioid receptors in the body, triggering a rebound effect that stimulates endorphin production. These natural endorphins regulate the immune system, reduce inflammation and provide pain relief. This mechanism makes LDN a promising treatment option for individuals battling autoimmune diseases, chronic pain, gastrointestinal disorders and even mental health challenges.
Morley Baker, Shed founder and CEO, said: "LDN is an exciting addition to our holistic approach to health. With the addition of LDN, we're able to provide a comprehensive solution that not only helps patients manage weight but also supports their overall health by targeting chronic conditions that have long been difficult to treat."
LEO Pharma advances delgocitinib cream into phase 3 trial for lichen sclerosus
HistoIndex partners Houston Research Institute
Formosa Pharmaceuticals licenses APP13007 ophthalmic therapy to Samil for South Korea
Bambusa Therapeutics reports first patient dosed in proof-of-concept COPD trial
Elanco Animal Health's Befrena (tirnovetmab) receives USDA approval for canine dermatitis
Sanofi and Regeneron's Dupixent gains Japan approval for paediatric asthma patients aged 6 to 11
Aqualung Therapeutics' Phase 2a lung fibrosis study approved by US FDA
Alvotech launches first-in-market golimumab biosimilar in Europe
Physiomics secures follow-on UK contract for Phase 2 study support
RedHill Biopharma reports positive opaganib data in venetoclax-resistant CLL
InduPro secures strategic investment and collaboration with Sanofi to advance autoimmune therapy
Innovent Biologics reports first participant dosed in Phase 1 trial of IBI3011