MARKET

NVCT

NVCT

Nuvectis Pharma, Inc.
NASDAQ
6.82
+0.10
+1.49%
After Hours: 6.82 0 0.00% 16:02 04/19 EDT
OPEN
6.68
PREV CLOSE
6.72
HIGH
6.85
LOW
6.44
VOLUME
44.46K
TURNOVER
0
52 WEEK HIGH
18.65
52 WEEK LOW
6.20
MARKET CAP
121.18M
P/E (TTM)
-4.7662
1D
5D
1M
3M
1Y
5Y
Weekly Report: what happened at NVCT last week (0408-0412)?
Weekly Report · 4d ago
Analysts Offer Insights on Healthcare Companies: Nuvectis Pharma (NVCT) and Invivyd (IVVD)
TipRanks · 04/08 16:10
Nuvectis Pharma: Data Confirms Robust Activity Of NXP900 - Quick Facts
NASDAQ · 04/08 13:08
Nuvectis Pharma's NXP900 Demonstrates Robust Activity In Non-Small Cell Lung Cancer Cell Lines
Highly Synergistic Antiproliferative Activity in EGFR-resistant Cells in Combination with Osimertinib, the Active Ingredient in TagrissoTM Single Agent Activity in Cells Resistant to Alectinib in NSCLC cells.
Benzinga · 04/08 12:41
NUVECTIS PHARMA INC: SINGLE AGENT ANTIPROLIFERATIVE ACTIVITY IN CELLS RESISTANT TO ALECTINIB, ACTIVE INGREDIENT IN ALECENSA
Reuters · 04/08 12:30
Weekly Report: what happened at NVCT last week (0401-0405)?
Weekly Report · 04/08 09:53
Weekly Report: what happened at NVCT last week (0325-0329)?
Weekly Report · 04/01 09:53
Weekly Report: what happened at NVCT last week (0318-0322)?
Weekly Report · 03/25 09:54
More
About NVCT
Nuvectis Pharma, Inc. is a clinical-stage biopharmaceutical company focused on the development of precision medicines for the treatment of serious conditions of unmet medical need in oncology. The Company is developing two drug candidates: NXP800 and NXP900. NXP800 is an oral small molecule GCN2 activator, which is in a Phase 1b clinical trial for the treatment for platinum resistant, ARID1a-mutated ovarian carcinoma and in an investigator-sponsored clinical trial for the treatment of cholangiocarcinoma. NXP800 activates the GCN2 kinase inducing inhibition of cap-dependent protein translation and activation of the integrated stress response leading to cancer cell death. NXP900 is a targeted-therapy, small molecule drug candidate that inhibits the proto-oncogene c-Src (SRC) and YES1 kinases, which is undergoing a Phase 1a dose escalation study. SRC is aberrantly activated in many cancer types, including solid tumor cancers such as breast, colon, prostate, pancreatic and ovarian cancers.

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