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Avacta Group Plc/£AVCT

1D1W1M3M6MYTD1Y5YMAX

About Avacta Group Plc

Avacta Group plc is a UK-based clinical-stage biopharmaceutical company focused on precision oncology therapies. Its core development platform, pre|CISION, uses a peptide linker designed to be cleaved by fibroblast activation protein, a protease associated with many solid tumours, with the aim of releasing cytotoxic payloads in the tumour microenvironment while reducing systemic exposure. The clinical pipeline includes faridoxorubicin (AVA6000), a tumour-activated form of doxorubicin, and AVA6103, a pre|CISION peptide drug conjugate incorporating exatecan. The company also owns the Affimer platform, comprising engineered binding proteins that can be used in therapeutic drug conjugates and diagnostic or research applications. Avacta is headquartered at Imperial College’s White City campus in London and has been transitioning to a pure-play oncology therapeutics business through the divestment of its diagnostics operations.
Ticker
£AVCT
Sector
Health
Primary listing
AIM
Employees
81
Website
avacta.com

Avacta Group Plc Metrics

BasicAdvanced
£263M
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-£0.09
-0.11
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What the Analysts think about Avacta Group Plc

Analyst ratings (Buy, Hold, Sell) for Avacta Group Plc stock.
Analyst projections of the future price of Avacta Group Plc stock.

Bulls say / Bears say

Faridoxorubicin’s Phase 1 study reported median progression-free survival of 11.4 months in a defined group of 32 salivary gland cancer patients, against historical benchmarks of 6–6.7 months. Three partial responses and six minor responses add an early efficacy signal in a rare cancer with limited treatment options. (Avacta Therapeutics)
AVA6103 has shown clinical proof of mechanism: its early pharmacokinetic results matched preclinical modelling, with controlled exatecan release lasting for days. It was well tolerated through the first three dose levels, including a payload dose about 50% above the maximum tolerated dose of conventional exatecan. (Avacta Therapeutics)
The FDA has agreed certain pivotal-trial elements and a regulatory path using Phase 1b data for potential full approval of faridoxorubicin. That clarity could help Avacta advance its lead drug towards a registration strategy, subject to the data supporting it. (Avacta Therapeutics)
Avacta remains dependent on external funding: it reported a £19.0 million net loss for H1 2026 and cash of £10.59 million at the end of August. The October raise extended its stated runway only into Q2 2027, so further financing may be needed before the business can generate meaningful revenue. (Avacta Therapeutics, Avacta Therapeutics)
The £12.5 million October fundraise issued new shares at 68 pence, diluting existing holders, and about £2.5 million of the proceeds was earmarked for a convertible-bond repayment. Repeated reliance on equity to fund trials and debt obligations could weigh on per-share value. (Avacta Therapeutics)
The 11.4-month progression-free survival result comes from a small, selected, non-randomised subset and is compared with historical results, not a control group. Only three of the 32 patients had partial responses, and median overall survival had not been reached, leaving the strength of the clinical benefit uncertain. (Avacta Therapeutics)
Data summarised monthly by Lightyear AI. Last updated on 8 Nov 2026.

Avacta Group Plc Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Avacta Group Plc Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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