Investment company IP Group plc (LSE: IPO) announced on Wednesday that its portfolio company Microbiotica Ltd has reported positive results from its Phase 1b first-in-human COMPOSER-1 trial of MB310 in patients with ulcerative colitis, highlighting the potential for a new non-immunosuppressive treatment modality aimed at delivering prolonged remission.
Cambridge-based Microbiotica announced on 11 February 2026 that the randomised, double-blind, placebo-controlled study in 29 patients with active, mild-to-moderate disease met its primary and secondary endpoints for safety, tolerability and engraftment, while demonstrating statistically significant efficacy signals versus placebo.
Clinical remission was achieved in 63.2% of MB310-treated patients compared with 30.0% in the placebo arm. All treated patients who entered follow-up remained in sustained remission, with complete resolution of rectal bleeding. Treatment also improved histological markers of mucosal damage and reduced faecal calprotectin levels. Rapid engraftment of all eight bacterial strains was observed and maintained throughout the 12-week dosing and 12-week follow-up periods. Safety profile and withdrawal rates were comparable to placebo.
MB310 is an investigational, once-daily oral live biotherapeutic product designed to restore gut barrier integrity without immune suppression. Microbiotica plans to advance the programme into an adaptive Phase 2/3 trial in combination with anti-inflammatory and/or immune-modulatory induction agents.
IP Group plc holds an undiluted 16.7% beneficial stake in Microbiotica, valued at GBP13.9m as at 30 June 2025.
Microbiotica, spun out of the Wellcome Sanger Institute in 2016, has raised more than GBP62m in equity funding, including a GBP50m Series B in 2022, and is developing programmes in immuno-oncology and inflammatory bowel disease.
Vir Biotechnology's VIR-5500 receives FDA Fast Track designation for prostate cancer
Voyager signs cancer research mission management contract
AstraZeneca completes USD2bn equity investment in Summit Therapeutics
GE HealthCare to acquire SOFIE Biosciences for USD945m
Avimer Bio and CNIO publish JACS study on computational design of self‑assembling protein cages
MHRA approves Zepzelca and atezolizumab as first-line maintenance therapy for ES-SCLC in the UK
AstraZeneca invests USD2bn in Summit Therapeutics to advance ADC and cancer-drug combinations
Fuse Oncology and Associated Medical Professionals of NY launch FuseRx proof of concept
Leo Cancer Care invests in children's experience of radiotherapy, following world-first treatments
Innovent expands global Phase 3 study of IBI363/TAK-928 to include non-squamous NSCLC
FDA approves WELIREG and LENVIMA combination for previously treated advanced renal cell carcinoma
AstraZeneca's IMFINZI combination receives US Priority Review for muscle-invasive bladder cancer
UChicago Medicine completes construction phase of new cancer facility
FDA Advisory Committee votes in favour of GRAIL's Galleri multi-cancer early detection test