TransThera Sciences (Nanjing) (2617) H1 2026 earnings summary
Event summary combining transcript, slides, and related documents.
H1 2026 earnings summary
13 Oct, 2026Executive summary
H1 revenue was RMB35.455m, entirely from a one-time upfront Neurocrine NLRP3 licensing payment; net loss narrowed to RMB95.465m from RMB122.866m YoY.
Tinengotinib received conditional China marketing approval on 6 August 2026 for previously treated FGFR2-altered CCA; overseas Phase III enrollment was completed.
H1-end cash and time deposits totaled RMB924.7m, following three H-share placements that raised net proceeds of ~HK$624m.
The pipeline included six clinical-stage candidates plus preclinical programs, while commercial team, channel and supply-chain preparations advanced.
Financial highlights
Revenue was RMB35.455m in H1 2026 versus nil in H1 2025, from a non-refundable, non-creditable upfront payment under the Neurocrine NLRP3 license and collaboration agreement.
Gross profit was RMB35.455m; net loss was RMB95.465m versus RMB122.866m YoY, and basic and diluted loss per share was RMB0.24 versus RMB0.32.
R&D costs rose 11.7% to RMB109.9m; administrative expenses fell 16.1% to RMB23.1m, partly reflecting lower one-off listing costs.
Other income increased to RMB14.0m, including RMB9.0m in government grants; other expenses rose to RMB11.9m, mainly from RMB11.7m net FX losses.
Outlook and guidance
Priorities include domestic confirmatory and overseas registrational Phase III development for CCA, plus Tinengotinib Phase II combination studies in prostate, breast and liver cancers.
Commercial launch preparations include hospital access, channel coverage, out-of-hospital networks, team build-out and compliant operating systems; commercial operations are planned in line with regulatory progress.
Further development includes TT-00973 with firmonertinib in NSCLC and TT-01488 with anti-CD20 therapy in MCL; preclinical programs target oncology, inflammation and metabolic diseases.
Remaining proceeds from the 2025 global offering are expected to be fully utilized by end-2027; placement proceeds have utilization timelines extending through 2028, 2029 and 2030.