已收盤 01-09 16:10:00
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证券之星消息,截至2025年12月31日收盘,时富投资(01049.HK)报收于1.06港元,与上一交易日持平,成交量24.0股,成交额22.0港元。
2025-12-31 18:51
香港联交所最新资料显示,12月10日,董事长关百豪增持时富投资(01049)1.8万股,每股作价1.03港元,总金额约为1.85万港元。
2025-12-11 18:53
证券之星消息,截至2025年11月27日收盘,时富投资(01049.HK)报收于0.78港元,与上一交易日持平,成交量5.0股,成交额4.0港元。
2025-11-27 18:58
时富投资(01049.HK)发布公告,于2025年10月22日,财丰有限公司(本公司的全资附属公司)作为租户与代理万泰拓展(作为业主的代理)(独立第三方)订立有关续租该等物业(九龙九龙湾宏泰道23号Manhattan Place 28楼全层)作为本集团办公室用途的要约的续租要约书。
2025-10-22 16:56
Celcuity Inc. announced positive Phase 3 results for gedatolisib in treating HR+/HER2-/PIK3CA wild-type advanced breast cancer. The gedatolisib triplet and doublet demonstrated significant improvements in median progression-free survival (PFS) compared to fulvestrant, with reductions in disease progression or death risk by 76% and 67%, respectively. The safety profile was favorable, with low-grade treatment-related adverse events (TRAEs) and low ...
2025-10-18 08:30
Celcuity Inc. announced the full enrollment of the PIK3CA mutant cohort in their Phase 3 VIKTORIA-1 clinical trial and provided updated analysis from a Phase 1b trial. The Phase 1b trial showed a median progression-free survival (PFS) of 14.6 months for HR+/HER2-/PIK3CA-mutated advanced breast cancer patients treated with gedatolisib, fulvestrant, and palbociclib. The Phase 3 trial expects to report topline data in late Q1 or early Q2 2026.
2025-10-18 08:30
<p>Cellebrite (NASDAQ: CLBT), a leader in digital investigative solutions, announced it will release its third-quarter 2025 financial results after the U.S. market close on November 12, 2025. Later that day, the company will host a conference call and webcast at 5:00 p.m. ET to discuss the results and provide a full-year 2025 outlook. Details include a call-in number (203-518-9814 / 800-274-8461) with conference ID CLBTQ325, and webcast links ava...
2025-10-17 13:00
Cellectis reported promising Phase 1 data for lasme-cel (UCART22) in relapsed/refractory B-cell acute lymphoblastic leukemia (r/r B-ALL). The study showed an overall response rate (ORR) of 68% with Process 2 (n=22), 83% at the recommended Phase 2 dose (RP2D, n=12), and 100% in the target Phase 2 population (n=9). Safety was generally well-tolerated with manageable adverse events. In the Phase 2 population, 56% achieved complete remission (CR)/CR ...
2025-10-16 19:19
<b>Event Summary:</b> Cellectis is hosting an R&D Day in New York City to present full Phase 1 data and discuss the pivotal Phase 2 strategy for lasme-cel (UCART22) in r/r B-ALL. <br><br> <b>Event Details:</b> October 16, 2025, 08:30 – 10:30 a.m. ET, in-person and live webcast available. <br> <br> <b>Cellectis Overview:</b> A clinical-stage biotech company developing allogeneic CAR T immunotherapies and gene therapies. <br><br> <b>Webcast:</b> Jo...
2025-10-16 11:00