logo
Canada's One and Only Aston Martin Valiant, delivered by Grand Touring Automobiles

Canada's One and Only Aston Martin Valiant, delivered by Grand Touring Automobiles

Globe and Mail11-04-2025
One of just 38 globally, V12 supercar was commissioned by F1 ® legend Fernando Alonso .
TORONTO , /CNW/ - Grand Touring Automobiles, Canada's foremost retailer of luxury and exotic vehicles, proudly announces the delivery of the Aston Martin Valiant — an ultra-exclusive, trackfocused, road-legal supercar and the sole unit allocated to the Canadian market. With global production limited to just 38 examples, the arrival of Valiant marks a rare and prestigious moment in the Canadian automotive landscape.
Born from a personal commission by two-time FIA Formula One® World Champion and Aston Martin's Aramco Formula 1 ® Team driver, Fernando Alonso , and brought to life by Q by Aston Martin — the marque's in-house bespoke division — Valiant is a bold celebration of power, precision, and purposeful design. Fitted with a formidable 734-hp 5.2-litre, twin-turbocharged V12 engine and paired with a sixspeed manual transmission, this limited-edition vehicle seamlessly marries motorsport engineering with the artistry of modern coachbuilding with a full-carbon fiber body.
"Delivering Canada's only Aston Martin Valiant is a true honour," said Paul Cummings , Dealer Principal and CEO of Grand Touring Automobiles. "This vehicle represents the highest expression of Aston Martin's technical mastery and bespoke craftsmanship. It is also a testament to our unwavering commitment to offering our clients access to the most exceptional and rare vehicles in the world."
Finished in a striking bespoke Golden Saffron exterior and adorned with exclusive Q Commission badging, Valiant is further distinguished by Alonso's signature hand-applied to the centre console — a personal touch that solidifies its place in automotive history.
"The Aston Martin Valiant is more than a performance vehicle — it is an embodiment of the brand's racing heritage and bespoke philosophy," said Alek A. Ackerman , Aston Martin Brand Manager. "It's a collector-grade car designed for driving purists, blending visceral performance with a unique aesthetic tailored for the most discerning enthusiasts."
The arrival of Valiant further strengthens Grand Touring Automobiles' position as Canada's premier destination for exclusive automotive experiences. This delivery not only exemplifies the company's dedication to excellence but also reinforces its ongoing relationship with world-class automotive brands that continue to redefine the boundaries of luxury and performance.
For more information on Grand Touring Automobiles' exclusive superluxury and hyperluxury offerings, or to inquire about bespoke vehicle commissions, please contact: Mario Cipollone by email mcipollone@grandtouringautos.com or by phone at 416.540.3353.
About Grand Touring Automobiles
Grand Touring Automobiles is Canada's premier retailer of luxury automobiles. The luxury and exotic brands represented include Aston Martin, Bentley , Bugatti, Hennessey, Hedley Studios, Himalaya, Jaguar, Land Rover, Koenigsegg, Lamborghini, Lotus, Pininfarina, Polestar, RIMAC, Rolls-Royce Motor Cars, and Zagato. It is the stage upon which each brand portrays its unique interpretation of refinement, sophistication, safety, and style—a collection unmatched in Canada , and presented by a dedicated curator seeking the ultimate automobile experience for discerning customers. With Ontario locations in Toronto , Vaughan , and Oakville , and Alberta locations in Calgary , Grand Touring Automobiles proudly offers Canada's largest and best selection of luxury and exotic cars. GrandTouringAutomobiles.com
Connect with us on social: instagram.com/grandtouringautos | tiktok.com/@grandtouringauto | facebook.com/GrandTouringAutomobiles | linkedin.com/company/grand-touring-automobiles/
Photo credits: Nathaniel Cooper and Alphi Masivi.
Note to Editors: High-resolution images, interviews, and additional information are available at gtamedia.ca with videos and additional assets available upon request.
SOURCE Grand Touring Automobiles
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Health Canada Approves KEYTRUDA® for the treatment of adult patients with FIGO 2014 Stage III-IVA cervical cancer, in combination with chemoradiotherapy (CRT)¹ Français
Health Canada Approves KEYTRUDA® for the treatment of adult patients with FIGO 2014 Stage III-IVA cervical cancer, in combination with chemoradiotherapy (CRT)¹ Français

Cision Canada

time26 minutes ago

  • Cision Canada

Health Canada Approves KEYTRUDA® for the treatment of adult patients with FIGO 2014 Stage III-IVA cervical cancer, in combination with chemoradiotherapy (CRT)¹ Français

KIRKLAND, QC, July 21, 2025 /CNW/ -- Merck (NYSE: MRK), known as MSD outside of the United States and Canada, announced today that Health Canada has granted approval for KEYTRUDA ® (pembrolizumab), Merck's anti-PD-1 therapy, in combination with chemoradiotherapy (CRT) for the treatment of FIGO (International Federation of Gynecology and Obstetrics) 2014 Stage III-IVA cervical cancer. 1,2 The approval is based on data from the Phase 3 KEYNOTE-A18 trial, also known as ENGOT-cx11/GOG-3047, which demonstrated statistically significant improvements in progression-free survival (PFS) and overall survival (OS) in patients randomized to KEYTRUDA ® in combination with CRT compared with patients randomized to placebo plus CRT. 3 "The approval of KN-A18 is an important addition to the treatment of gynecological cancers, as it has demonstrated a statistically significant improvement in overall survival and progression-free survival in patients with FIGO 2014 Stage III-IVa," stated Shannon Salvador, Gynecologic Oncologist at the Jewish General Hospital and President of the Society of Gynecologic Oncology of Canada. 4"This recent approval adds another therapeutic option for patients in an important disease space." "This approval marks a pivotal moment for patients, as it represents the first indication in Canada for KEYTRUDA ® in combination with chemoradiotherapy," said André Galarneau, PhD, Executive Director & Vice President, Oncology Business Unit at Merck Canada. "Reaffirming our commitment to cervical cancer, we are eager to continue expanding treatment options for patients impacted by this disease." 5 About KEYNOTE-A18 / ENGOT-cx11/GOG-3047 KEYNOTE-A18 is a multicenter, randomized, double-blind, placebo-controlled phase III trial ( NCT04221945). 2 The trial investigated the efficacy of pembrolizumab in combination with CRT (cisplatin and external beam radiation therapy [EBRT] followed by brachytherapy [BT]) for the treatment of patients with locally advanced cervical cancer. 1 The trial enrolled 1,060 newly diagnosed patients with locally advanced squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma of the cervix defined as FIGO 2014 stage IB2 to IIB with positive lymph nodes or stage III to IVA regardless of nodal status. 3 There were 599 patients with FIGO 2014 Stage III-IVA. Randomization was stratified by planned type of EBRT (Intensity modulated radiation therapy [IMRT] or volumetric modulated arc therapy [VMAT] vs. non IMRT and non VMAT), stage at screening of cervical cancer (FIGO 2014 Stage IB2 IIB vs. FIGO 2014 Stage III-IVA), and planned total radiotherapy dose (EBRT + brachytherapy dose of <70 Gy vs. ≥70 Gy as per equivalent dose [EQD2]). 1 Patients were randomized (1:1) to one of two treatment arms: Pembrolizumab 200 mg IV every 3 weeks (5 cycles) concurrent with cisplatin 40 mg/m2 IV weekly (5 cycles, an optional sixth infusion could be administered per local practice) and radiotherapy (EBRT followed by BT), followed by pembrolizumab 400 mg IV every 6 weeks (15 cycles). 1,3 Placebo IV every 3 weeks (5 cycles) concurrent with cisplatin 40 mg/m2 IV weekly (5 cycles, an optional sixth infusion could be administered per local practice), and radiotherapy (EBRT followed by BT), followed by placebo IV every 6 weeks (15 cycles). 1,3 Treatment continued until RECIST (Response Evaluation Criteria in Solid Tumors) v1.1-defined progression of disease as determined by investigator or unacceptable toxicity. 1 Assessment of tumour status was performed every 12 weeks from completion of CRT for the first two years, followed by every 24 weeks in year 3, and then annually. The major efficacy outcome measures were PFS as assessed by investigator according to RECIST v1.1, modified to follow a maximum of 10 target lesions and a maximum of 5 target lesions per organ, or histopathologic confirmation, and OS. 1 The trial demonstrated statistically significant improvements in both PFS (HR (Hazard Ratio) 0.70; 95% CI (confidence interval): 0.55–0.89; p = 0.002) and OS (HR 0.67; 95% CI: 0.50–0.90; p = 0.004) in the overall population. In an exploratory subgroup analysis for the 459 patients (43%) with FIGO 2014 Stage IB2–IIB disease, the PFS and OS HR estimates were 0.91 (95% CI: 0.63–1.32) and 0.89 (95% CI: 0.55–1.44), respectively, suggesting that the improvements in PFS and OS observed in the overall population were primarily driven by the later-stage subgroup of patients with FIGO 2014 Stage III–IVA disease. The efficacy results in the exploratory subgroup analysis of 599 patients with FIGO 2014 Stage III-IVA disease showed that pembrolizumab plus CRT demonstrated improvements in PFS (Hazard Ratio (HR) 0.59; 95% CI 0.43, 0.81) and OS (HR 0.58; 95% CI 0.40, 0.85) in the overall population. 1 For the FIGO 2014 Stage III-IVA population, the most common treatment-related adverse events (reported in at least 20% of patients) were anemia, nausea, diarrhea, white blood cell count decreased, neutrophil count decreased, vomiting, platelet count decreased, and hypothyroidism. 6 For complete information, refer to the KEYTRUDA ® product monograph. About cervical cancer Cervical cancer forms in the cells lining the cervix, which is the lower part of the uterus. 7 Despite concerted efforts in screening and prevention across Canada, cervical cancer has become the fastest growing cancer type in females. 8,9 In 2024 alone, it was estimated that there were approximately 1,600 women diagnosed with cervical cancer and an estimated 400 deaths as a result of the disease. 10 About KEYTRUDA ® KEYTRUDA ® is an anti-programmed death receptor-1 (anti-PD-1) therapy that works by helping increase the ability of the body's immune system to help detect and fight tumour cells. KEYTRUDA ® is a humanized monoclonal antibody that blocks the interaction between PD-1 and its ligands, PD-L1 and PD-L2, thereby activating T lymphocytes which may affect both tumour cells and healthy cells. 11,12,13 KEYTRUDA ® was first approved in Canada in 2015 and currently has indications in several disease areas, including advanced renal cell carcinoma, bladder cancer, non-small cell lung carcinoma, primary mediastinal B-cell lymphoma, classical Hodgkin lymphoma, colorectal cancer, endometrial carcinoma, cervical cancer, esophageal cancer, triple-negative breast cancer, melanoma, and head and neck squamous cell carcinoma. 14 About Merck At Merck, known as MSD outside of the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable, and healthy future for all people and communities. For more information about our operations in Canada, visit and connect with us on LinkedIn @MerckCanada. Forward-Looking Statement of Merck & Co., Inc., Rahway, N.J., USA This news release of Merck & Co., Inc., Rahway, N.J., USA (the "company") includes "forward-looking statements" within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. These statements are based upon the current beliefs and expectations of the company's management and are subject to significant risks and uncertainties. There can be no guarantees with respect to pipeline candidates that the candidates will receive the necessary regulatory approvals or that they will prove to be commercially successful. If underlying assumptions prove inaccurate or risks or uncertainties materialize, actual results may differ materially from those set forth in the forward-looking statements. Risks and uncertainties include but are not limited to, general industry conditions and competition; general economic factors, including interest rate and currency exchange rate fluctuations; the impact of pharmaceutical industry regulation and health care legislation in the United States and internationally; global trends toward health care cost containment; technological advances, new products and patents attained by competitors; challenges inherent in new product development, including obtaining regulatory approval; the company's ability to accurately predict future market conditions; manufacturing difficulties or delays; financial instability of international economies and sovereign risk; dependence on the effectiveness of the company's patents and other protections for innovative products; and the exposure to litigation, including patent litigation, and/or regulatory actions. The company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise. Additional factors that could cause results to differ materially from those described in the forward-looking statements can be found in the company's Annual Report on Form 10-K for the year ended December 31, 2023 and the company's other filings with the Securities and Exchange Commission (SEC) available at the SEC's Internet site ( ® Merck Sharp & Dohme LLC. Used under license. © 2025 Merck & Co., Inc., Rahway, NJ, USA and its affiliates. All rights reserved. CA-NON-04142 1 KEYTRUDA ® Product Monograph, page 285-286. 2 3 The ASCO Post. KEYNOTE-A18: Overall Survival in Cervical Cancer Improved by Pembrolizumab Plus Chemoradiotherapy. 4 Pembrolizumab or placebo with chemoradiotherapy followed by pembrolizumab or placebo for newly diagnosed, high-risk, locally advanced cervical cancer (ENGOT-cx11/GOG-3047/KEYNOTE-A18): overall survival results from a randomised, double-blind, placebo-controlled, phase 3 trial, page 1329. 5 6 KEYTRUDA ® Product Monograph, page 146. 7 Canadian Cancer Society. What is cervical cancer? 8 Canadian Cancer Statistics 2023, page 22. 9 Canadian Cancer Statistics 2023, page 80. 10 Canadian Cancer Society. Cervical cancer statistics. 11 KEYTRUDA ® Product Monograph, page 300. 12 KEYTRUDA ® Product Monograph, page 188. 13 KEYTRUDA ® Product Monograph, page 192. 14 KEYTRUDA ® Product Monograph, pages 1-3. Media Contacts: Merck Canada Media Relations 1-833-906-3725 [email protected]

Business confidence subdued amid tariffs but ‘worst-case' less likely: BoC survey
Business confidence subdued amid tariffs but ‘worst-case' less likely: BoC survey

Winnipeg Free Press

time26 minutes ago

  • Winnipeg Free Press

Business confidence subdued amid tariffs but ‘worst-case' less likely: BoC survey

A pair of reports from the Bank of Canada say tariff-related uncertainty continued to put a damper on business and consumer sentiment in the second quarter, but the worst-case trade scenarios previously anticipated seem less likely. The central bank's business outlook survey said 28 per cent of firms are now planning for a recession in Canada, down from 32 per cent last quarter but still up from 15 per cent over the previous two quarters. Sales outlooks remain pessimistic overall due to widespread concerns about the effects of a slowing economy, but the report says recent monthly surveys suggest some improvement in firms' outlooks, especially among exporters because few have been directly affected by current tariffs. Meanwhile, the Canadian survey of consumer expectations says spending intentions have weakened further because of persistent tariff threats. Consumers also continue to see the labour market as soft amid 'elevated' fears of job loss. Monday Mornings The latest local business news and a lookahead to the coming week. The reports come ahead of the Bank of Canada's next interest rate decision and monetary policy report set for July 30. This report by The Canadian Press was first published July 21, 2025.

TSX Edges Higher Amid Mixed Commodity Signals
TSX Edges Higher Amid Mixed Commodity Signals

The Market Online

timean hour ago

  • The Market Online

TSX Edges Higher Amid Mixed Commodity Signals

The TSX is creeping higher this morning as investors brace for the Bank of Canada's Business Outlook Survey—digging for clues on how corporate Canada's really feeling under the weight of tariff turmoil. Market Numbers (Futures) TSX : Up ( 0.02%) 27,368.64TSXV: Up (0.77%%) 797.75DOW: Up (0.23%) 44,641.00NASDAQ: Up (0.25%) 23,281.25 FTSE: Down (0.10%) 8,982.96 In the Headlines: With a high-stakes vote on the horizon, Canadians are questioning whether Canada Post still matters in a digital age, or if it's just snail mail dragging its feet. And Alaska Airlines resumes operations after it shakes off a massive tech meltdown that grounded its entire fleet, rebooting operations but leaving travel chaos in its wake. Currencies Update: (Futures) The Canadian dollar dips 0.19% to $0.7313 cents U.S., but it holds a firmer line against the euro down 0.18% to $0.6244. Meanwhile, Bitcoin inches higher by 0.44%, landing at C$163,150.67 Commodities: (Futures) Natural Gas: Down: Up (4.46%), 3.41WTI: Up (0.04%), 67.33Gold: Up (0.77%), 3,376.49 Copper: Up (0.36%) 6.05 To stay up-to-date on all of your market news head to Join the discussion: Find out what everybody's saying check out the rest of Stockhouse's stock forums and message boards. The material provided in this article is for information only and should not be treated as investment advice. For full disclaimer information, please click here

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store