NeuClone Reports Dosing of NeuLara (proposed biosimilar- ustekinumab) in P-I Trial
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- Australian Therapeutic Goods Administration (TGA) Clinical Trial Notification (CTN) scheme is responsible for conducting the NeuLara P-I trial and is being conducted across 200 healthy volunteers assessing PK and safety of US- and EU-sourced Stelara
- NeuClone’s NeuLara is the second biosimilar in pipeline to enter in clinical development and is developed in partnership with Serum Institute of India
- NeuLara is a mAb targeting interleukin-12 and -23 developed to treat patients with plaque psoriasis- psoriatic arthritis- Crohn’s disease- and ulcerative colitis
Click here to read full press release/ article | Ref: NeuClone | Image: Twitter
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