TOFACITINIB SETS THE BENCHMARK.
How does YOUR COMPOUND COMPARE?

Proven clinical efficacy. Proven preclinical translation.

Newsletter # 138



In vivo studies


How do you know your next arthritis candidate has real therapeutic potential?

Before entering costly development stages, compounds must demonstrate efficacy in predictive preclinical models. Neurofit's Pristane-Induced Arthritis (PIA) rat model provides the dynamic range needed to identify meaningful therapeutic effects and differentiate promising candidates from the rest.
Tofacitinib has become one of the most widely used targeted therapies for rheumatoid arthritis. When evaluated in Neurofit's PIA model, this clinically validated benchmark compound produced a clear and robust dose-dependent response, reducing disease burden by up to 91%.
UP TO 91% REDUCTION IN ARTHRITIS DISEASE LOAD

  • NEUROFIT website
  • NEUROFIT website
Why This Matters for Your Drug Candidate
An actionable screening platform must do more than separate active from inactive molecules. It must deliver the dynamic range needed to:
■ Detect partial efficacy across early-stage hits,
■ Demonstrate true dose-response relationships,
■ Differentiate subtle efficacy gaps between competing leads,
■ Support rationale-backed lead selection and dose optimization,
■ Generate investor-ready proof-of-concept data.

The Neurofit PIA model consistently delivers high-translatability insights, making it an ideal platform for benchmarking:
■ Small molecules & targeted kinase inhibitors,
■ Biologics & monoclonal antibodies,
■ Novel immunomodulators,
■ First-in-class anti-inflammatory agents.
Available inflammatory disease models:
■ Pristane-Induced Arthritis (PIA),
■ Collagen-Induced Arthritis (CIA,)
■ Oxazolone-Induced Dermatitis,
■ Ovalbumin-Induced Allergic Inflammation.



NEUROFIT offers a range of validated in vitro and in vivo screening tests for psychiatry and neurology.

If you need further information, please do not hesitate to contact us, we will reply within few days. Custom protocol

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