Channel Therapeutics Corp

Channel Therapeutics Corp(CHRO)股票分析

$13.500

+0.964 (+7.14%)收盤時

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High
14.800
Open
14.000
VWAP
13.53
Vol
19.48K
Mkt Cap
Low
12.301
Amount
263.70K
EV/EBITDA, TTM
0.00

Channel Therapeutics Corporation is engaged in developing innovative, non-addictive, drugs to treat chronic neuropathic and acute and chronic eye pain. The Company is focused on the development of non-opioid pain treatment therapeutics with a focus on modulating NaV1.7 receptors responsible for sensing and transmitting pain in the peripheral nervous system. It is initially targeting orphan chronic pain indications, specifically small fiber neuropathy and erythromelalgia, and acute and chronic eye pain. The Company’s patented, selective, and potent (nM) inhibitor of human NaV1.7 has demonstrated additional efficacy in several models of pain: acute, chronic, inflammatory, visceral, post-surgical, and chemotherapy-induced.

估值指標

The current forward P/E ratio for Channel Therapeutics Corp (CHRO) is -1.45, compared to its 5-year average forward P/E of -1.28.

Forward P/E

Fair
5Y Average P/E
-1.28
Current P/E
-1.45
高估
-0.65
低估
-1.92

Forward EV/EBITDA

Strongly Undervalued
5Y Average EV/EBITDA
0.00
Current EV/EBITDA
0.00
高估
0.00
低估
0.00

Forward P/S

Strongly Undervalued
5Y Average P/S
0.00
Current P/S
0.00
高估
0.00
低估
0.00

事件時間軸

2025-05-14 (ET)

08:14:35

Channel Therapeutics announces efficacy results for eye drop formulations

2025-04-17 (ET)

06:03:55

Ligand subsidiaries, Chromocell Therapeutics to merge

2024-12-20 (ET)

08:10:58

Channel Therapeutics highlights difference between NaV1.7, NaV1.8

2024-12-18 (ET)

07:33:37

Channel Therapeutics announces data for formulation of NaV1.7 inhibitor

2024-11-21 (ET)

08:52:35

Chromocell changes name to Channel Therapeutics, provides program updates

資訊

CHRO FAQ — answered by Alphio AI

Channel Therapeutics Corporation is engaged in developing innovative, non-addictive, drugs to treat chronic neuropathic and acute and chronic eye pain. The Company is focused on the development of non-opioid pain treatment therapeutics with a focus on modulating NaV1.7 receptors responsible for sensing and transmitting pain in the peripheral nervous system. It is initially targeting orphan chronic pain indications, specifically small fiber neuropathy and erythromelalgia, and acute and chronic eye pain. The Company’s patented, selective, and potent (nM) inhibitor of human NaV1.7 has demonstrated additional efficacy in several models of pain: acute, chronic, inflammatory, visceral, post-surgical, and chemotherapy-induced. It operates in the Healthcare sector (BIOLOGICAL PRODUCTS, EXCEPT DIAGNOSTIC SUBSTANCES industry).

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