已收盘 08-22 16:00:00 美东时间
+0.530
+8.36%
近日,各大机构向美国证券交易委员会(SEC)陆续提交13F报告,披露了二季度所持美股股票和持仓规模。 其中,股神巴菲特15.7亿重仓医疗巨头、继续减持苹果,高瓴...
08-15 09:16
H.C. Wainwright analyst Joseph Pantginis reiterated a Buy rating on Nuvectis Ph...
08-12 22:15
The Phase 1b program is designed to evaluate the clinical activity of NXP900 as a single agent in patients with advanced solid tumors whose cancers harbor specific genetic alterations, and in combination with EGFR and
08-12 04:44
Nuvectis Pharma announced the initiation of the Phase 1b program for NXP900, focusing on evaluating its efficacy as a single agent in advanced solid tumors with specific genetic alterations and in combination with EGFR/ALK inhibitors for NSCLC patients resistant to these treatments. The program includes a single-agent component targeting YES1 amplified or FAT1 mutated NSCLC, NF2 mutated mesothelioma and renal cancer, and other solid tumors with r...
08-11 20:30
Nuvectis Pharma reported successful completion of NXP900's Phase 1a and drug-drug interaction studies, advancing to Phase 1b, with a strengthened cash position of $39 million after ATM share acquisition. The company plans to explore NXP800 in additional cancer types. Net loss for Q2 2025 was $6.3 million, with cash increasing to $26.8 million due to public offerings. Stock closed at $7.60, up 13.4% from $6.71.
08-05 11:30
Gainers Psyence Biomedical (NASDAQ:PBM) stock rose 62.6% to $8.78 during Thurs...
07-31 20:08
As part of the NXP800 Phase 1b study, 17 patients with recurrent, platinum resistant, ARID1a-mutated ovarian cancer were treated with NXP800 at the target dose of 75 mg/day, administered intermittently or daily, with
07-31 19:48
Nuvectis Pharma provided updates on NXP800 and NXP900. NXP800 showed partial responses and stable disease in ovarian cancer, with thrombocytopenia managed via intermittent dosing. The company is evaluating its potential in other cancers. NXP900 completed successful DDI and Phase 1a studies, with plans for Phase 1b initiation soon. The company prioritizes advancing NXP900 while exploring NXP800 opportunities elsewhere.
07-31 11:45
Nuvectis Pharma announced successful completion of a DDI study for NXP900, a weak CYP3A inhibitor, supporting its potential as a combination partner with EGFR/ALK inhibitors for NSCLC. The study in 14 healthy volunteers showed NXP900 increased Midazolam levels by <2-fold, with no serious adverse events reported. This data supports advancing NXP900 into Phase 1b trials, targeting cancers sensitive to SRC/YES1 inhibition, leveraging its unique mech...
07-08 12:00
Nuvectis Pharma ( ($NVCT) ) just unveiled an update. On June 12, 2025, Nuvectis...
06-14 05:37