Recent 8-K filings for CNTB
Highest-materiality recent filing
Connect Biopharma private placement $20.2M; Phase 1 IV rademikibart shows rapid bronchodilation; Phase 3 AD efficacy
- Raised $20.2M via private placement of 6.13M shares at $3.25; led by Panacea Venture; extends cash runway into H2 2027.
- Phase 1 IV rademikibart: rapid FEV1 improvements of 200-400 mL within 15 mins in asthma/COPD, maintained through Day 29.
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Connect Biopharma Q2 net loss $17.3M; enrollment done in both Seabreeze STAT trials
Q2 2026 net loss $17.3M ($0.27/share) vs $12.9M ($0.23) in Q2 2025; H1 loss $36.7M ($0.61).
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Connect Biopharma FY2025 net loss $55.5M; cash runway extended by $20.2M placement
Net loss FY2025 $55.5M ($1.00 per share) vs $15.6M ($0.28 per share) in FY2024.
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Raised $20.2M via private placement of 6.13M shares at $3.25; led by Panacea Venture; extends cash runway into H2 2027.
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Connect Biopharma Q3 net loss $17.2M; cash $54.8M; Seabreeze STAT studies on track for 1H26 topline
Net loss of $17.2M ($0.31 per share) in Q3 2025 vs $12.9M ($0.23) in Q3 2024; 9-month net loss $40.4M ($0.73) vs $6.7M ($0.12).
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Connect Biopharma Q2 net loss $12.9M; cash $71.8M; ADR program termination planned
Net loss $12.9M ($0.23) vs net income $14.8M ($0.27) in Q2 2024; revenue $48K vs $24.1M.
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Connect Biopharma regains Nasdaq minimum bid price compliance; delisting risk removed
Received Nasdaq letter on July 17, 2025 confirming compliance with Minimum Bid Price Requirement.
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Connect licensee Simcere submits NDA for rademikibart in China for atopic dermatitis
Simcere submitted NDA to NMPA for rademikibart to treat atopic dermatitis in adults and adolescents.
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Connect Biopharma Q1 net loss $10.3M; cash $84M; initiates two Phase 2 rademikibart trials
Cash, equivalents and ST investments $84.0M as of March 31, 2025; runway into 2027.
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Connect Biopharma starts Phase 2 COPD study of rademikibart, topline data expected 1H 2026
Phase 2 Seabreeze STAT COPD study initiated after FDA agreement on final protocol.
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Phase 2 Seabreeze STAT Asthma study (NCT06940141) initiated after FDA agreement on final protocol.
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Connect Biopharma gains FDA alignment for Phase 2 trials of rademikibart in acute asthma/COPD
FDA Type C meeting positive; agency aligned on parallel Phase 2 trials for rademikibart in acute exacerbations of asthma or COPD.
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Connect Biopharma reports FY2024 net loss $15.6M; cash $93.7M into 2027
Revenue $26.0M from Simcere license; no revenue in FY2023.
Earnings & guidance
Materiality & sentiment trend
Max materiality 0.80 · Median 0.60 · Most common event earnings