
B.C. grocer avoids selling U.S. produce for 117 days in what expert calls a ‘real' boycott
Garth Green, general manager of Urban Grocer, says when U.S. Donald Trump launched his trade war on Canada in March, they decided to pull all U.S.-grown produce from the shelves.
And so far, it's been a big success.
'We're, you know, just really trying to promote the local farms,' he said.
'And the Canadian farms. And so it's been very, very good for us. The customers have been very appreciative of it.'
The experiment has not been without its challenges.
When Green found out they could only get cauliflower from the U.S., he realized it was currently cauliflower season in Holland.
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'So we reached out to a few suppliers and said, 'Hey, can you get Holland cauliflower for us?'' he said.
'We ended up finding some, brought it in, and you know it's a little bit more expensive to bring in because you're flying it in. But we just took, you know, a less margin, sell it at a regular price and be able to give the customer something that they can buy until B.C. cauliflower was available.'
6:19
50% tariffs to hit Canadian copper imports to the U.S.
Green said local farmers are now reaching out to offer produce to their customers.
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'There's people every day almost that come in here and say, 'You know, we hear what you're doing and we love it and we'd love to join on board with you and really shop here,''' he added.
Green added that it is unfortunate that it took something like the trade war to make this change but he is happy it has been so successful.
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'We've got a Canada-first motto that we like to push, but, you know, we're also not blind to the fact that you can't get everything from Canada, right?' he said.
'And so, you know, even across the store, we are working towards trying to go all Canadian if possible. It's going to be a lot harder, but we've started the process and started to weed out some of the suppliers that we don't need.'
0:27
Business response to Trump's 35% tariff threat
Sylvain Charlebois, with the Faculty of Management at Dalhousie University, researches food distribution, security and safety.
He told Global News that what Urban Grocer is doing points to a broader movement against American products at the grocery store.
'What's really interesting is that people haven't really boycotted chains like Walmart or Costco, but they're boycotting products,' he said.
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'And the boycott naturally worked. If you look at the data, not surveys, actual sales data, according to NielsenIQ, by volume, sales for American food products are down about 8.5 per cent.'
Charlebois said in the food retail business, that number is huge.
'That's a boycott. That's the boycott now,' he added.
Charlebois added that while consumers are seeing fewer U.S. products, they are seeing more products from around the world so it does not necessarily mean that Canadian product companies are benefiting from the boycott.
'The boycott is absolutely real. So this boutique store is a good, strong case study for what actually is happening across the country.'
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Toronto Sun
23 minutes ago
- Toronto Sun
'Persistent lack of good faith engagement': Couche-Tard abandons $11B takeover of 7-Eleven owner
Canadian convenience store giant says it received 'no sincere or constructive engagement' from Seven & i Holdings Published Jul 16, 2025 • Last updated 30 minutes ago • 2 minute read Quebec-based Alimentation Couche-Tard has withdrawn its proposed acquisition of Seven & i Holdings Co., the Japanese parent company of 7-Eleven, after months of what it described as limited cooperation. In a scathing letter on Wednesday and addressed to Seven & i's board of directors, the Laval-based retailer said it was stepping back from its ¥2,600-per-share all-cash offer, worth approximately $11 billion, due to 'a persistent lack of good faith engagement.' 'We continue to believe that a combination of Seven & i Holdings and Alimentation Couche-Tard would create a global leader in convenience,' the letter said. 'However, we are not able to effectively pursue this combination without deeper and genuine further engagement.' This advertisement has not loaded yet, but your article continues below. THIS CONTENT IS RESERVED FOR SUBSCRIBERS ONLY Subscribe now to read the latest news in your city and across Canada. Unlimited online access to articles from across Canada with one account. Get exclusive access to the Toronto Sun ePaper, an electronic replica of the print edition that you can share, download and comment on. Enjoy insights and behind-the-scenes analysis from our award-winning journalists. Support local journalists and the next generation of journalists. Daily puzzles including the New York Times Crossword. SUBSCRIBE TO UNLOCK MORE ARTICLES Subscribe now to read the latest news in your city and across Canada. Unlimited online access to articles from across Canada with one account. Get exclusive access to the Toronto Sun ePaper, an electronic replica of the print edition that you can share, download and comment on. Enjoy insights and behind-the-scenes analysis from our award-winning journalists. Support local journalists and the next generation of journalists. Daily puzzles including the New York Times Crossword. REGISTER / SIGN IN TO UNLOCK MORE ARTICLES Create an account or sign in to continue with your reading experience. Access articles from across Canada with one account. Share your thoughts and join the conversation in the comments. Enjoy additional articles per month. Get email updates from your favourite authors. THIS ARTICLE IS FREE TO READ REGISTER TO UNLOCK. Create an account or sign in to continue with your reading experience. Access articles from across Canada with one account Share your thoughts and join the conversation in the comments Enjoy additional articles per month Get email updates from your favourite authors Don't have an account? Create Account Couche-Tard said its proposal, submitted earlier this year, represented a 47.6 per cent premium to Seven & i's unaffected share price. It said the offer was fully financed and included a plan to obtain regulatory approvals, particularly in the United States. The company stated it had entered into a non-disclosure agreement with Seven & i following an April 18 meeting in Tokyo but had since received 'no sincere or constructive engagement… contrary to comments made publicly by 7&i representatives, including in the July 11, 2025 earnings call in which 7&i noted it is 'seriously' considering our proposal.' It also alleged that Seven & i had 'engaged in a calculated campaign of obfuscation and delay.' Couche-Tard said it received just 14 files relating to Seven & i's U.S. operations over a 10-week period and that 'none of our critical questions were answered.' It also said two management meetings—one in Dallas and one in Tokyo—yielded limited insights, with executives declining to answer key questions. Your noon-hour look at what's happening in Toronto and beyond. By signing up you consent to receive the above newsletter from Postmedia Network Inc. Please try again This advertisement has not loaded yet, but your article continues below. 'At the Dallas meeting… the content of the meeting was, as your advisor characterized it, a 'readout,'' the letter stated. 'When one 7-Eleven executive attempted to thoughtfully address a question… he was interrupted and rebuked by Mr. Dacus who pointed to his head as if to remind his colleague to 'think.' Mr. Dacus also declared in the meeting that the discussion was a management presentation and 'not due diligence.'' On regulatory issues, Couche-Tard said it had proposed a term sheet with specific store divestiture plans and a reverse termination fee worth over $1.4 billion, but that Seven & i 'was not willing to share the required information with potential buyers.' In a bid to find common ground, Couche-Tard said it proposed acquiring 100 per cent of Seven & i's non-Japanese operations and 40 per cent of its domestic business, leaving 60 per cent with existing shareholders. This advertisement has not loaded yet, but your article continues below. However, it said Seven & i instead proposed contributing its U.S. business into Couche-Tard in exchange for equity, which Couche-Tard argued would not deliver the 'significant premium' its proposal offered and would 'undermine the operational prospects of the combined business.' The company concluded: 'We remain as excited as ever about the path forward for (Alimentation Couche-Tard)… However, we are not able to effectively pursue this combination without deeper and genuine further engagement from 7&i leadership and the special committee. Accordingly, we are withdrawing our proposal at this time.' Couche-Tard operates nearly 17,000 stores across 29 countries and territories, under the Circle K and Couche-Tard banners, and employs approximately 146,000 people. It is one of the largest independent convenience store operators in the U.S. Its founder, Alain Bouchard, is the richest man in Quebec, according to The Gazette Rich List. 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Globe and Mail
23 minutes ago
- Globe and Mail
Toronto sixplex policy ‘disappointing,' Federal Housing Minister says
Federal Housing Minister Gregor Robertson says he's unhappy with Toronto's move to limit sixplexes, and that the policy falls short of the housing commitment he expects from Canada's most-populous city. But in an interview with The Globe and Mail, the former Vancouver mayor declined to get into specifics about how his department will respond to Toronto's action beyond saying talks are under way on the issue. 'The decision on sixplexes is disappointing and not in line with the ambition that we expect from Toronto,' Mr. Robertson said on Wednesday. 'My focus is working with partners at every level of government and using every tool we have available to tackle the housing crisis, and we need to see that from our biggest city.' Mr. Robertson declined to say whether he would follow the policy of former housing minister, Nate Erskine-Smith, who warned Toronto Mayor Olivia Chow that any deviation from a citywide policy permitting such buildings would result in 25 per cent less federal funding. On housing, Toronto fails a crucial test That would have meant about $30-million of $118-million that Ottawa has pledged annually to Toronto from its Housing Accelerator Fund, a multibillion-dollar program announced in the 2021 election by the Liberals under Justin Trudeau that's intended to create a greater supply of affordable housing. 'I won't share details,' Mr. Robertson said on the question of a punitive response against Toronto. 'We have some time before a decision has to be made regarding funding. That's the rest of the year to find solutions on this, but it's certainly disappointing.' In late June, Toronto City Council passed a motion allowing property owners in nine of the city's 25 wards to build up to six units on one lot without additional permission. The initial plan to allow sixplexes citywide was amended because of fears that it did not have majority support and would be shot down. The sixplex policy was one of eight 'milestones' in an agreement between Toronto and the federal government that promised the city $471-million over four years. Toronto Mayor confident city's compromise on sixplexes won't risk federal housing funding Ms. Chow had told a recent meeting with the editorial board of The Globe and Mail that, as a former mayor, Mr. Robertson understands the challenges raised by municipal politics. But Mr. Robertson was sharply critical of Toronto's move. He said there is a lot of misinformation about sixplexes or fourplexes that ignores the reality that neighborhoods already have multiunit homes that fit into their fabric. 'I think that this decision got made without the clarity that this is the gentle density we need in single family home neighbourhoods,' he said. He said there are many big homes with multiple units that would not be easily identified as sixplex units. The minister said fourplexes and sixplexes are becoming the norm in cities all over the world. He also noted that the the federal government has signed more than 240 agreements through its housing fund. 'We must see that leadership in Toronto. We're seeing it across the country in hundreds of other communities.' In response to Mr. Robertson, Ms. Chow's press secretary said the mayor has taken an energetic approach to dealing with housing. A statement issued by Zeus Eden said Ms. Chow has been a champion for middle and affordable housing by supporting such housing options as fourplexes, under certain conditions, laneway and garden suites and mid-rise apartment buildings on major avenues. 'We are working closely with Minister Gregor and city councillors to advance ambitious housing policy,' he said.


Cision Canada
an hour ago
- Cision Canada
Cancer Pipeline Milestones Coming Fast as Regulators Revisit Research Priorities
Issued on behalf of Oncolytics Biotech Inc. VANCOUVER. BC, July 16, 2025 /CNW/ -- As lawmakers weigh potential cuts to scientific research funding, the outlook for developing cancer cures faces growing uncertainty. The situation is further complicated by renewed regulatory scrutiny of mRNA vaccines at both federal and state levels, casting a shadow over ongoing cancer research efforts. Meanwhile, the incidence of cancers—especially gastrointestinal and colorectal cancers among younger populations—is on the rise, heightening the need for new therapeutic approaches. In response, a new generation of biotech companies is stepping forward with promising clinical milestones on the horizon, including Oncolytics Biotech Inc. (NASDAQ: ONCY) (TSX: ONC), Zai Lab Limited (NASDAQ: ZLAB), GeoVax Labs, Inc. (NASDAQ: GOVX), OS Therapies (NYSE-American: OSTX), and SELLAS Life Sciences Group, Inc. (NASDAQ: SLS). Industry forecasts suggest the global oncology drug market could climb past US$900 billion by 2034. Within that, next-generation cancer treatments —powered by advances in personalized and precision medicine—are expected to reach US$175.2 billion, according to Precedence Research, growing at a compound annual rate of 7.35%. Oncolytics Biotech Inc. (NASDAQ: ONCY) (TSX: ONC) just rolled out an expanded translational data review package that tightens the scientific case for pelareorep, its intravenously delivered oncolytic virus. Fresh analyses from the GOBLET gastrointestinal‑cancer study and the AWARE‑1 breast‑cancer study shows pelareorep actively replicating inside tumors, switching on interferon signaling in the immune system, and drawing tumor‑infiltrating lymphocytes into the cancer microenvironment. "This robust data set, amassed from several studies in cancers that have historically resisted immunotherapeutic approaches, provides definitive validation of pelareorep's immune-mediated mechanism of action," said Dr. Thomas Heineman, Chief Medical Officer of Oncolytics. "We observed tumor biopsy-confirmed virus replication, immune cell activation, and the recruitment of cytotoxic T cells into the TME – all consistent with the durable responses observed in patients with metastatic PDAC and HR+/HER2- breast cancer who were treated with pelareorep." Investigators also recorded a clear increase in PD‑L1 expression, a checkpoint marker that helps immune cells recognize tumors, and tracked newly expanded T‑cell clones in the blood that matched those inside shrinking lesions. Together, these findings suggest pelareorep can convert "cold" tumors into "hot" ones that respond better to modern immunotherapies. "The collection of data here show that pelareorep works how a cancer immunotherapy should work," said Jared Kelly, CEO of Oncolytics. "Pelareorep is a versatile product candidate with strong platform potential to enhance immunological responses in multiple indications, including hard-to-treat cancers. Such compelling findings should be exciting to strategic partners focused on finding a platform immunotherapy in large indications with high unmet medical needs." Two GOBLET cohorts—metastatic pancreatic ductal adenocarcinoma (mPDAC) and anal cancer—remain open. Management plans to outline the next clinical milestones before the end of the third quarter. Clinical outcomes already hint at real‑world benefit. In more than 100 first‑line mPDAC patients, pelareorep‑based regimens achieved a two‑year overall‑survival rate of 21.9%, compared with the historical benchmark of 9.2%. A separate single‑arm study that paired pelareorep with chemotherapy and a checkpoint blocker produced a 62% objective response rate. No immune checkpoint therapy is approved in this cancer today, which makes the signal especially noteworthy. Progress extends to hormone‑receptor‑positive, HER2‑negative metastatic breast cancer (HR+/HER2‑ mBC). Across two randomized trials, pelareorep added more than ten months of median overall survival. In BRACELET‑1, the drug nearly doubled median progression‑free survival to 12.1 months versus 6.4 months in the control arm, suggesting durable disease control. Next week, Oncolytics will host a KOL webinar on July 22 featuring leading GI and immuno-oncology experts to discuss pelareorep's data and positioning in pancreatic and gastrointestinal cancers. Participating physicians include the GOBLET trial's primary investigator as well as global leaders in immunotherapy and clinical trial design, underscoring the growing interest in pelareorep's mechanism and outcomes. To steer these data toward value‑creating deals and late‑stage trials, Oncolytics Biotech strengthened its leadership earlier this year. The board tapped industry veteran Jared Kelly for the CEO seat and named Andrew Aromando Chief Business Officer. Both executives helped guide Ambrx Biopharma into a $2‑billion sale to Johnson & Johnson, giving them a playbook for capital‑efficient development and strategic partnering. "Pelareorep's clinical data across multiple tumors is striking and represents the potential for a true backbone immunotherapy to address many in-need indications," said Kelly. "With a renewed focus and sharpened clinical development plan, we believe we will move pelareorep forward effectively and efficiently to a place where potential partners will see the value of a de-risked immunotherapy." As CBO, Aromando is now leading global business development and helping shape the company's corporate, clinical, and regulatory strategies. The leadership tandem is expected to prioritize partnering and expansion opportunities while preserving capital efficiency—a strategy well-suited for pelareorep's growing clinical profile. "I'm thrilled to join Oncolytics at such a pivotal moment in its evolution," said Aromando. "With promising data in difficult-to-treat cancers and a compelling body of clinical evidence in over 1,100 patients, I believe the Company is uniquely positioned to deliver meaningful value to patients and other stakeholders in the near term." Pelareorep currently holds FDA Fast Track designation in both mPDAC (pancreatic cancer) and HR+/HER2- mBC (breast cancer), with Orphan Drug status for pancreatic cancer in the U.S. and Europe. In other recent industry developments and happenings in the market include: Zai Lab Limited (NASDAQ: ZLAB) recently reported that its Phase 3 FORTITUDE‑101 study found bemarituzumab plus mFOLFOX6 significantly improved overall survival over chemotherapy alone in first‑line fibroblast growth factor receptor 2b (FGFR2b)‑positive gastric and gastroesophageal junction cancers. The antibody becomes the first FGFR2b inhibitor to post a statistically and clinically meaningful survival benefit, and the company plans a rapid regulatory filing in China under its Breakthrough Therapy designation. "Bemarituzumab is the first FGFR2b inhibitor to demonstrate a statistically and clinically significant overall survival benefit in a randomized Phase 3 trial for the first-line treatment of FGFR2b-positive gastric cancer," said Dr. Rafael Amado, M.D., President, Head of Global Research and Development at Zai Lab. "The success of the global Phase 3 FORTITUDE-101 study highlights the potential of bemarituzumab to redefine the standard of care for a patient population that has faced poor outcomes with existing therapies. We are proud to have contributed meaningfully to this pivotal trial, including a substantial number of patients enrolled in China. Based on these results, and the regulatory Breakthrough Designation, we plan to move rapidly toward regulatory submission in China to bring this transformative therapy to patients as quickly as possible." GeoVax Labs, Inc. (NASDAQ: GOVX) recently stated that the FDA's curative‑intent approval of Keytruda for head and neck cancer strengthens the rationale for its planned Phase 2 trial combining Gedeptin and pembrolizumab. "We believe Gedeptin's tumor-targeted cytotoxicity can enhance immunotherapy efficacy, particularly in the perioperative window where anti-tumor immunity can be primed," added Dr. Kelly McKee, GeoVax's Chief Medical Officer. "We are excited to embark on the next phase of Gedeptin development as we attempt to build on the important advances being made in this disease." The study, expected to launch in 2026, will give Gedeptin intratumorally before surgery to trigger local cytotoxicity, then add checkpoint inhibition to boost systemic immunity. Endpoints include pathologic response, recurrence rates, and immune biomarkers, aligning with guidance in a recent New England Journal of Medicine editorial. OS Therapies (NYSE-American: OSTX) has locked in an End‑of‑Phase 2 FDA meeting for 27 August 2025 to discuss a rolling Biologics License Application for OST‑HER2 in recurrent, lung‑metastatic osteosarcoma, while parallel regulatory consultations are set with the EMA and the UK MHRA. "We are making significant progress towards our primary objective of obtaining regulatory approval for OST-HER2 in recurrent, pulmonary metastatic osteosarcoma prior to the sunsetting of the rare pediatric disease priority review voucher ("PRV") program," said Paul Romness, MPH, Chairman & CEO of OS Therapies. "We strongly believe in the promise of the listeria immunotherapy platform to help prevent and treat cancer, and intend to judiciously deploy our capital to focus on the OST-HER2 approval while advancing our other clinical programs without deploying significant capital or running other clinical studies while we wait for the OST-HER2 approval and related PRV sale." The company is also advancing a Phase 1 prostate‑cancer immunotherapy, OST‑504, with full data expected later in 2025. OST‑HER2 already carries Rare Pediatric Disease, Fast Track, and Orphan Drug designations, positioning the program for a potential Priority Review Voucher and accelerated approvals in multiple markets. SELLAS Life Sciences Group, Inc. (NASDAQ: SLS) met every primary endpoint in its Phase 2 trial of SLS009 in relapsed/refractory acute myeloid leukemia-myelodysplasia-related changes (AML MR), delivering a 44% overall response rate at the optimal 30 mg twice‑weekly dose and a median overall survival of 8.9 months—far above the 2.4 month historical benchmark. The CDK9 inhibitor also showed a 50% response rate in high‑risk ASXL1‑mutated and M4/M5 subgroups, with no dose‑limiting toxicities reported. "We are excited to report that our Phase 2 trial met all key endpoints, with clinical responses and survival outcomes that exceed targeted expectations and historical benchmarks," said Angelos Stergiou, MD, ScD h.c., President and CEO of SELLAS. "AML remains an area of urgent unmet medical need, particularly for patients with relapsed or refractory disease, where standard treatments are often ineffective and poorly tolerated. What sets SLS009 apart is its consistent efficacy across a broad range of molecular subtypes." Following FDA guidance, the company will launch an 80‑patient randomized study in newly diagnosed first‑line AML by Q1 2026 to support a potential New Drug Application. DISCLAIMER: Nothing in this publication should be considered as personalized financial advice. We are not licensed under securities laws to address your particular financial situation. No communication by our employees to you should be deemed as personalized financial advice. Please consult a licensed financial advisor before making any investment decision. This is a paid advertisement and is neither an offer nor recommendation to buy or sell any security. We hold no investment licenses and are thus neither licensed nor qualified to provide investment advice. The content in this report or email is not provided to any individual with a view toward their individual circumstances. Equity Insider is a wholly-owned subsidiary of Market IQ Media Group, Inc. ("MIQ"). MIQ has been paid a fee for Oncolytics Biotech Inc. advertising and digital media from the company directly. There may be 3rd parties who may have shares of Oncolytics Biotech Inc., and may liquidate their shares which could have a negative effect on the price of the stock. This compensation constitutes a conflict of interest as to our ability to remain objective in our communication regarding the profiled company. Because of this conflict, individuals are strongly encouraged to not use this publication as the basis for any investment decision. The owner/operator of MIQ own shares of Oncolytics Biotech Inc. which were purchased in the open market, and reserve the right to buy and sell, and will buy and sell shares of Oncolytics Biotech Inc. at any time without any further notice commencing immediately and ongoing. We also expect further compensation as an ongoing digital media effort to increase visibility for the company, no further notice will be given, but let this disclaimer serve as notice that all material, including this article, which is disseminated by MIQ has been approved by Oncolytics Biotech Inc.; this is a paid advertisement, we currently own shares of Oncolytics Biotech Inc. and will buy and sell shares of the company in the open market, or through private placements, and/or other investment vehicles. 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