Northwire Canada EditionSunday, October 18, 2026
Northwire
⌕
GOLD 4181.10 +0.3% SILVER 57.30 +0.3% COPPER 6.57 +0.3% OIL 99.02 +1.1% PALLADIUM 1118.60 −0.9% GBU 0.095 +0.0% ATY 0.225 +4.7% GRDM 0.215 +0.0% PPM 0.300 +0.0% GZD 0.040 −11.1% CAN 0.060 +0.0% BGF 0.025 +0.0% MSV 0.570 +0.0% CCMM 0.485 +0.0% MON 0.385 −6.1% OMI 0.245 −2.0% BUFF 0.800 +2.6% FEO 0.630 −3.1% LIB 0.710 −1.4% NPR 0.620 +0.0% QZM 0.380 +0.0% GOLD 4181.10 +0.3% SILVER 57.30 +0.3% COPPER 6.57 +0.3% OIL 99.02 +1.1% PALLADIUM 1118.60 −0.9% GBU 0.095 +0.0% ATY 0.225 +4.7% GRDM 0.215 +0.0% PPM 0.300 +0.0% GZD 0.040 −11.1% CAN 0.060 +0.0% BGF 0.025 +0.0% MSV 0.570 +0.0% CCMM 0.485 +0.0% MON 0.385 −6.1% OMI 0.245 −2.0% BUFF 0.800 +2.6% FEO 0.630 −3.1% LIB 0.710 −1.4% NPR 0.620 +0.0% QZM 0.380 +0.0%
Financings

Cardiol Therapeutics Completes US$11.4 Million Financing and Extends Cash Runway into Q3 2027

CRDL · Price

Executive Summary

  • Cardiol Therapeutics completed a private placement raising US $11.4 million, providing funding to support operations into Q3 2027 and accelerate development of its heart‑failure programs.
  • The company highlighted positive Phase II ARCHER trial results showing a significant reduction in left‑ventricular mass, supporting further orphan‑drug designation for CardiolRx™ and advancing the next‑generation CRD‑38 formulation.
  • Ongoing pivotal Phase III MAVERIC trial for recurrent pericarditis is fully funded through to a planned New Drug Application submission with the FDA.

Key Details

  • Financing Structure: 11.4 million Units sold at US $1.00 per Unit. Each Unit includes one Class A common share and half of a common‑share purchase warrant.
  • Warrant Terms: Whole warrants allow purchase of one additional common share at an exercise price of US $1.35, exercisable for 24 months; acceleration clause triggers expiry 30 days after a news release if the VWAP exceeds US $2.00 for five consecutive trading days.
  • Use of Proceeds: Expected to fund corporate operations and clinical programs through Q3 2027, including Phase III MAVERIC trial and development of CRD‑38.
  • Clinical Highlights – ARCHER Trial: Demonstrated a marked reduction in LV mass, the first structural/remodeling improvement evidence in myocarditis patients; data to be presented at a cardiology conference in November 2025.
  • Regulatory Status: CardiolRx™ holds Orphan Drug Designation for recurrent pericarditis from the U.S. FDA.
  • Future Plans: Pursuing additional orphan‑drug designation for CardiolRx™ in myocarditis; advancing CRD‑38 subcutaneous formulation toward broader heart‑failure market.
  • Related‑Party Participation: Insiders participated in the offering; transaction deemed a related‑party transaction under MI 61‑101, exempt from formal valuation and minority‑shareholder approval because fair market value did not exceed 25 % of market cap.

Notable Quotes

“As recruitment in our pivotal Phase III MAVERIC trial gains momentum… we are pleased to have secured a direct investment of US$11.4 million to strengthen our balance sheet and accelerate the development of our novel heart failure drug, CRD‑38,” – David Elsley, President & CEO, Cardiol Therapeutics.


All forward‑looking statements are subject to risks and uncertainties detailed in the release.

Read the original news release →

More from CARDIOL THERAPEUTICS INC. CL 'A'