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Zacks Small-Cap Research repeats its valuation on Tiziana Life Sciences PLC as company starts nasally administered Foralumab trial for SPMS

Zacks Small-Cap Research repeats its valuation on Tiziana Life Sciences as company starts nasally administered Foralumab trial for SPMS Tiziana Life Sciences is advancing three candidates for a variety of indications in autoimmune disease, cancer and coronavirus (COVID-19) Tiziana announced, on May 25, it had begun treating a first patient with secondary progressive multiple sclerosis (SPMS) in a trial using nasally administered Foralumab - its fully-human anti-CD3 monoclonal antibody Zacks Small-Cap Research has put out a note on drug developer Tiziana Life Sciences PLC (NASDAQ:TLSA) (LON:TILS), which it started covering in April this year, repeating its valuation of US$7.50 per ADR share, compared to a current price of US$2.37.

Psyence Group Inc is finalizing agreements with partners in Jamaica to develop its natural psilocybin-based formulations

Tiziana Life Sciences PLC hails major accomplishment as nasally administered antibody shows potential to treat degenerative diseases such as MS

The latest data come from a phase I assessment of Foralumab, which is being developed for a range of diseases

4D pharma PLC encouraged after additional analysis of IBS drug data

4D pharma encouraged after additional analysis of IBS drug data Presented as a poster at the medical and scientific conference, Digestive Disease Week, the new analysis builds on the top-line results released last October 4D pharma PLC (LON:DDDD, NASDAQ:LBPS) said it has provided a more detailed analysis of its Live Biotherapeutic, Blautix, which is both significant and supportive of its continued development as an irritable bowel syndrome treatment. The data, presented as a poster at the medical and scientific conference Digestive Disease Week, builds on the top-line results released last October. The poster revealed “strong and statistically significant activity” on the key symptom of bowel habit, which 4D describes as a “potential approvable primary endpoint per regulatory guidelines”.

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