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SOLASTA Bio files first US product and posts strong field demo under heavy whitefly pressure

6 hours ago
SOLASTA Bio files first US product and posts strong field demo under heavy whitefly pressure
By AI, Created 17:19 UTC, Oct 28, 2026, AGP -

SOLASTA Bio has submitted its first peptide-based insecticide for US registration, with EPA and California regulators now reviewing the package. The company also said a Georgia field demo showed visible crop protection performance during a whitefly surge not seen locally in more than a decade.

Why it matters: - SOLASTA Bio is trying to bring a peptide-based insecticide platform into the US market with a faster regulatory path than conventional chemistry. - The first filing targets aphids in leafy greens and vegetable crops, where resistance and tighter limits on traditional insecticides are increasing pressure on growers. - The field demo suggests the lead product can perform under severe pest pressure, a key hurdle for commercial adoption.

What happened: - SOLASTA Bio submitted regulatory packages for its peptide active ingredient and first end-use product to the US Environmental Protection Agency and the California Department of Pesticide Regulation. - The lead product is now under concurrent review by both regulators. - The submission follows the EPA's classification of SOLASTA Bio's lead peptide as a biochemical, which can support a faster and more cost-effective review than conventional insecticides. - The company hosted investors and partners in Georgia in early October for its second field demonstration event.

The details: - The first registration is aimed at aphid control in leafy greens and vegetable crops. - SOLASTA Bio's lead active ingredient is a nature-identical peptide selected for consistent aphid efficacy across multiple crops in field and greenhouse trials. - The peptide has a benign ecotoxicology profile, does not bioaccumulate, and showed no impact on beneficial species or plant health. - SOLASTA Bio is also seeking recognition from the Insecticide Resistance Action Committee for the technology as an entirely new mode of action. - The company said that designation would give US growers another option for rotating products to manage pest resistance. - The Georgia demo included field evaluations against aphids and whiteflies, plus selected peptides targeting Lepidoptera on different crops. - Local whitefly populations were reported at levels not seen in more than a decade. - Across the aphid, whitefly and lepidopteran evaluations, treated plots showed visible reductions in leaf-feeding damage and clearer improvements in plant vigor, health and appearance. - Visitors saw the treatment differences first-hand in the field. - SOLASTA Bio also cited a growing portfolio of US, European and rest-of-world patents. - The company completed an oversubscribed $14 million Series A funding round in 2024. - Backers in that round included Forbion BioEconomy Fund, Corteva Catalyst and FMC Ventures.

Between the lines: - SOLASTA Bio is positioning its technology as both a crop-protection tool and a resistance-management tool, which matters as aphids and whiteflies become harder to control. - The company is using field performance under extreme pest pressure to support its commercialization story, not just its regulatory case. - The combination of patent coverage, outside investment and active regulatory review suggests the company is moving from research toward market entry.

What's next: - The EPA and California regulators will continue reviewing the registration packages. - SOLASTA Bio will likely push for IRAC recognition and prepare for the commercial rollout of its first product if approvals move forward. - The company's pipeline is expected to follow its lead product as it moves toward commercialization.

The bottom line: - SOLASTA Bio has crossed a key US regulatory threshold and is now trying to prove its peptide insecticide can scale from promising field data to commercial farm use.

Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.

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