0001601830-26-000097
SEC filingRecursion二季度营收降至$7.7M、净亏损收窄至$131.0M,Genentech首个神经科学靶点进入早期发现项目成头号驱动。
| 指标 | 本期 | 去年同期 | 同比 |
|---|---|---|---|
| Total revenue | $7.7 million | $19.2 million | — |
| Operating revenue | $7.3 million | $19.1 million | — |
| Grant revenue | $0.4 million | $0.1 million | — |
| Cost of revenue | $11.5 million | $20.2 million | — |
| Research and development | $89.6 million | $128.6 million | — |
| General and administrative | $41.5 million | $46.7 million | — |
| Loss from operations | $(135.0) million | $(176.2) million | — |
| Net loss | $(131.0) million | $(171.9) million | — |
| Net loss per share, basic and diluted | $(0.25) | $(0.41) | — |
| Cash operating expense (Non-GAAP, H1) | $191.0 million | $199.1 million | — |
| 期间 | 指标 | 指引 | 口径 |
|---|---|---|---|
| FY2026 | Cash operating expense | <$375 million(原<$390 million) | Non-GAAP |
本季营收降至$7.7 million,主因Roche与Genentech在上一期间完成部分项目阶段后确认收入减少;净亏损收窄至$131.0 million,每股亏损$(0.25)。费用端明显收缩:R&D降至$89.6 million,其中Tempus患者多模态肿瘤数据相关非现金支出由去年同期的$22.7 million降至$3.1 million;G&A降至$41.5 million,减少$5.1 million主要来自年内裁员带来的薪酬下降$4.9 million。经营现金流净流出扩大至$105.9 million,因去年同期含$28.6 million英国R&D税收抵免流入。
业务端,Genentech行使首个Validated Target Option,将此前未探索的神经科学靶点推进至小分子早期发现项目,公司称这是AI原生平台可发现并实验验证新靶点的早期证据;Roche/Genentech合作累计已实现$216 million前期及里程碑付款,Sanofi合作累计$134 million。REC-7735(PI3Kα H1047R)IND获批,Phase 1/2 ZINNIA试验将于2H26启动;REC-4881(MEK1/2)FAP新增Phase 2数据将于2026年11月CGA-IGC总统全会公布,FDA注册路径更新预计2H26。现金及等价物与受限现金$556.8 million(2025年末$753.9 million),在无新增融资下现金跑道延续至2028年初;全年现金运营费用指引下调$15 million至<$375 million,体现持续的经营效率改善。