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News | Mirriad Advertising rallies on Middle East contract news

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Mirriad Advertising rallies on Middle East contract news

38 Views / News Story by Advert On Click / 28 July 2025
Source: proactiveinvestors
Mirriad Advertising rallies on Middle East contract news

Mirriad Advertising PLC (AIM:MIRI, OTCQX:MMDDF) has entered into a two-year services agreement with MBC Media Solutions FZ-LLC. MBC is the advertising arm of MBC Group, a satellite broadcasting company operating in the Middle East and North Africa.

Under the deal, Mirriad will deliver virtual in-video advertising services across MBC’s subscription and linear platforms.

It sees a minimum purchase commitment of 4,000 seconds of integrated brand content per year – to generate at least US$370,000 annually.

Mirriad will be the exclusive virtual product placement provider for the initial contract term.

"Together with MBC, we've previously built out a compelling model for brands to scale virtual placement campaigns and planning in the Middle East, and it's great to renew and now formalise our partnership with a fresh sense of possibility with new offers in the region,” said chief executive Louis Wakefield.

In London, Mirriad shares rallied some 22% on Friday, trading up to 0.017p at one point, adding fresh impetus in what has been a challenging period for the adtech firm.

Previously, in June, Mirriad announced that Zeus Investment Management has acquired a significant stake in the company (just shy of 9%) and, in May, the firm secured £1.5 million of rescue funding after fears over its liquidity.

Genflow Biosciences PLC (LSE:GENF, OTCQB:GENFF) CEO Dr Eric Leire talked with Proactive's Stephen Gunnion about the company’s upcoming clinical trial application in Europe for its MASH (metabolic dysfunction-associated steatohepatitis) therapy, GF-1002.

Leire explained that Genflow is prioritising the European Medicines Agency over the FDA as it seeks clinical trial authorisation (CTA) for its GF-1002 programme. He emphasised the importance of this milestone in building company value, stating: “To have proof of efficacy in humans is super important for us to move as fast as possible to clinical trial authorisation.”

The company is working with Belgian-based CDMO Exothera on the CMC part of the filing, and Leire said results so far have exceeded expectations. He also highlighted the dual-CRO strategy involving Physiogenex and Accelera to address both early and late-stage MASH models. This approach aims to provide flexibility when engaging with regulators about the most effective path forward.

In a second update, Leire said the protocol for Genflow’s GF-1004 dog trial has been amended. The changes relate to the infusion rate of the gene therapy, intended to ensure consistency and future usability by private veterinarians. This is seen as a key step toward a potential partnership with an animal health company, which would bring non-dilutive funding to the business.

Leire also mentioned supportive market tailwinds from upcoming FCA regulatory changes.