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This is a list of investigational analgesics, or analgesics that are currently under development for clinical use but are not yet approved. Chemical/generic names are listed first, with developmental code names, synonyms, and brand names in parentheses.

Opioid receptor modulators

Sodium channel blockers

Calcium channel blockers

  • HSK16149 – selective ligand of α2δ subunit of voltage-gated calcium channel [9]

TRP channel modulators

Cannabinoid receptor modulators

Nerve growth factor inhibitors

Others

See also

References

  1. ^ "Drug profile | Axelopran/oxycodone". AdisInsight. Theravance Biopharma. 1 October 2021. Retrieved 29 October 2022.
  2. ^ "Drug profile | Cebranopadol". AdisInsight. Tris Pharma. 14 August 2022. Retrieved 29 October 2022.
  3. ^ "Drug profile | Desmetramadol". AdisInsight. Syntrix Biosystems. 5 October 2021. Retrieved 2 November 2022.
  4. ^ "Drug profile | Lexanopadol". AdisInsight. 20 August 2018. Archived from the original on 25 December 2018. Retrieved 2 November 2022.
  5. ^ "Drug profile | Oxycodone/naltrexone". AdisInsight. Elite Pharmaceuticals. 16 April 2021. Archived from the original on 14 November 2022. Retrieved 14 November 2022.
  6. ^ "Drug profile | BIIB 095". AdisInsight. Biogen. 7 May 2021. Archived from the original on 14 November 2022. Retrieved 14 November 2022.
  7. ^ Drug profile | CC 8464. Chromocell Corporation. 28 November 2019. Archived from the original on 15 March 2022. Retrieved 14 November 2022. {{ cite book}}: |work= ignored ( help)
  8. ^ "Drug profile | Cenobamate". AdisInsight. SK biopharmaceuticals. 28 November 2019. Archived from the original on 14 November 2022. Retrieved 14 November 2022.
  9. ^ Zaccara, Gaetano; Schmidt, D. (2017). "Antiepileptic Drugs in Clinical Development: Differentiate or Die?". Current Pharmaceutical Design. 23 (37). Bentham Science Publishers: 5593–5605. doi: 10.2174/1381612823666170809100524. eISSN  1873-4286. ISSN  1381-6128. PMID  28799516. S2CID  3676340.
  10. ^ Nakamura, Michiko; Shin, Hyewon; Jang, Il-Sung (26 April 2018). "Mechanism of Action of Cenobamate: Preferential Inhibition of the Persistent Sodium Current (P5.278)". Neurology. 90 (15 Supplement). doi: 10.1212/WNL.90.15_supplement.P5.278. eISSN  1526-632X. ISSN  0028-3878. LCCN  55043902. OCLC  960771045. S2CID  80887455.
  11. ^ "Drug profile | DSP 2230". AdisInsight. Sumitomo Dainippon Pharma. 4 April 2022. Archived from the original on 14 November 2022. Retrieved 14 November 2022.
  12. ^ Drug profile | Funapide. Xenon Pharmaceuticals. 6 September 2022. Archived from the original on 14 November 2022. Retrieved 14 November 2022. {{ cite book}}: |work= ignored ( help)
  13. ^ Nichols, Heather (19 July 2021). "Vertex Initiates Phase 2 Clinical Trial Program for VX-548 for the Treatment of Acute Pain". Vertex Pharmaceuticals (Press Release). Retrieved 14 November 2022. Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced that it has begun a Phase 2 proof-of-concept (POC) study in acute pain following bunionectomy surgery with the selective NaV1.8 inhibitor VX-548 and that it expects to commence a second Phase 2 study in acute pain following abdominoplasty surgery in the coming weeks.
  14. ^ Cross, Ryan (31 March 2022). "Vertex's non-opioid painkiller shows promise in people recovering from surgery". The Boston Globe. ISSN  0743-1791. OCLC  66652431. Archived from the original on 19 May 2022. Retrieved 14 November 2022. "There is an enormous need for novel non-opioid analgesics with no abuse liability," and Vertex's results are an "important advance," said Dr. Clifford J. Woolf, director of the F.M. Kirby Neurobiology Center and Boston Children's Hospital. It will be important for Vertex to determine whether the drug also works for patients with chronic pain, such as diabetic neuropathy and low back pain, "where the clinical need is highest," he added.
  15. ^ Manitpisitkul, Prasarn; Shalayda, Kevin; Russell, Lucille; Sanga, Panna; Solanki, Bhavna; Caruso, Joseph; Iwaki, Yuki; Moyer, John A. (10 November 2017). "Pharmacokinetics and Safety of Mavatrep (JNJ-39439335), a TRPV1 Antagonist in Healthy Japanese and Caucasian Men: A Double-Blind, Randomized, Placebo-Controlled, Sequential-Group Phase 1 Study". Clinical Pharmacology in Drug Development. 7 (7): 712–726. doi: 10.1002/cpdd.413. eISSN  2160-7648. ISSN  2160-763X. PMID  29125703. S2CID  11755963.
  16. ^ Manitpisitkul, Prasarn; Shalayda, Kevin; Russell, Lucille; Sanga, Panna; Williams, Yinka; Solanki, Bhavna; Caruso, Joseph; Moyer, John A. (2018). "Bioavailability and Pharmacokinetics of TRPV1 Antagonist Mavatrep (JNJ-39439335) Tablet and Capsule Formulations in Healthy Men: Two Open-Label, Crossover, Single-Dose Phase 1 Studies". Clinical Pharmacology in Drug Development. 7 (7): 699–711. doi: 10.1002/cpdd.412. ISSN  2160-7648. PMID  29125700. S2CID  32666782.
  17. ^ Moreno, Ana M.; Alemán, Fernando; Catroli, Glaucilene F.; Hunt, Matthew; Hu, Michael; et al. (10 March 2021). "Long-lasting analgesia via targeted in situ repression of NaV1.7 in mice". Science Translational Medicine. 13 (584). doi: 10.1126/scitranslmed.aay9056. eISSN  1946-6242. ISSN  1946-6234. PMC  8830379. PMID  33692134.

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