MARKET

CAMP

CAMP

Camp4 Therapeutics Corp.
NASDAQ
4.500
+0.170
+3.93%
After Hours: 4.500 0 0.00% 16:10 07/13 EDT
OPEN
4.280
PREV CLOSE
4.330
HIGH
4.604
LOW
4.280
VOLUME
108.13K
TURNOVER
--
52 WEEK HIGH
7.75
52 WEEK LOW
1.320
MARKET CAP
233.67M
P/E (TTM)
-2.0067
1D
5D
1M
3M
1Y
5Y
1D
Weekly Report: what happened at CAMP last week (0706-0710)?
Weekly Report · 14h ago
Weekly Report: what happened at CAMP last week (0629-0703)?
Weekly Report · 07/06 09:21
X4 Pharmaceuticals appoints CAMP4 Therapeutics CFO Kelly Gold to board
TipRanks · 07/01 11:20
X4 Pharmaceuticals appoints CAMP4 CFO Kelly Gold to board, audit committee
PUBT · 07/01 11:01
X4 PHARMACEUTICALS APPOINTS KELLY GOLD, EXPERIENCED CHIEF FINANCIAL OFFICER, TO ITS BOARD OF DIRECTORS
Reuters · 07/01 11:00
Weekly Report: what happened at CAMP last week (0622-0626)?
Weekly Report · 06/29 09:20
Analysts’ Top Healthcare Picks: TriSalus Life Sciences (TLSI), CAMP4 Therapeutics Corporation (CAMP)
TipRanks · 06/25 13:10
Positive Report for CAMP4 Therapeutics Corporation (CAMP) from J.P. Morgan
TipRanks · 06/23 12:37
More
About CAMP
CAMP4 Therapeutics Corporation is a clinical-stage biopharmaceutical company. The Company is focused on the discovery and development of regulatory RNA-based therapeutics with the goal of upregulating gene expression and restoring healthy protein levels to treat a range of genetic diseases. It is leveraging its RAP Platform to advance a pipeline of programs focused on metabolic and central nervous system (CNS) disorders with validated disease biology and potential market opportunities due to the significant unmet need of affected patients. Its lead product candidate, CMP-CPS-001, has the potential to be the first disease-modifying therapy for the treatment of urea cycle disorders. CMP-CPS-001 is designed to improve urea cycle activity by amplifying expression of CPS1, a key enzyme that catalyzes the first step of the urea cycle, by binding to a CPS1-specific regRNA. Its CNS development program, CMP-SYNGAP, is focused on addressing the underlying cause of SYNGAP1-related disorders.

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