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Co-Diagnostics (CODX) investor relations material
Co-Diagnostics Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Revenue for Q1 2026 was $146,000, up from $50,000 year-over-year, with most sales from the U.S. and a significant portion from a few customers.
Net loss widened to $9.1 million ($4.06 per share) from $7.5 million ($7.05 per share) year-over-year, driven by higher R&D and legal expenses and lower other income.
Advanced clinical and commercialization pipeline, focusing on upper respiratory multiplex and TB tests, and expanded international presence in India and Saudi Arabia.
Achieved key regulatory milestones, including CDSCO license and ISO 13485 certification for manufacturing in India, and initiated shipments of PCR Pro instruments and TB test materials.
Strengthened global presence through partnerships, distributor relationships, and participation in major industry events.
Financial highlights
Q1 2026 revenue was $146,000, up from $50,000 year-over-year; cost of revenue was $194,000, resulting in a gross loss of $48,000 versus a gross profit of $29,000 last year.
Operating expenses rose to $9.2 million from $8.6 million, mainly due to increased R&D and legal costs.
Net loss was $9.1 million ($4.06 per share) compared to $7.5 million ($7.05 per share) in Q1 2025.
Adjusted EBITDA loss was $8.7 million, up from $7.4 million year-over-year.
Cash and equivalents at quarter-end were $8.2 million, down from $11.9 million at 2025 year-end.
Outlook and guidance
Anticipates continued operating losses and cash use in the near term as investments in clinical pipeline and regulatory submissions persist.
Additional capital likely required to execute commercialization and development plans; evaluating equity, debt, and strategic partnerships.
Focus remains on disciplined capital allocation and securing non-dilutive funding, including grants.
FDA 510(k) submission for upper respiratory test expected in Q3 2026; TB clinical studies in India to begin imminently.
Substantial doubt exists about the ability to continue as a going concern for the next 12 months without new capital.
- AI-powered PCR platform offers rapid, affordable diagnostics and global market expansion.CODX
Investor presentation14 May 2026 - Shelf registration allows up to $150M in securities for diagnostics expansion and innovation.CODX
Registration filing12 May 2026 - Revenue fell to $0.6M, losses widened, but global expansion and regulatory progress continued.CODX
Q4 202531 Mar 2026 - Q2 revenue up, net loss narrowed, and FDA 510(k) submission advances new PCR platform.CODX
Q2 20242 Feb 2026 - Q3 revenue fell to $641K, net loss widened, but diagnostics pipeline and cash remain strong.CODX
Q3 202415 Jan 2026 - 2024 revenue fell and net loss widened as regulatory and manufacturing efforts progressed.CODX
Q4 202426 Dec 2025 - Annual meeting to vote on director, executive pay, and auditor, with board recommending all proposals.CODX
Proxy Filing2 Dec 2025 - Proxy covers director elections, equity plan, executive pay, and auditor ratification.CODX
Proxy Filing2 Dec 2025 - Q2 2025 revenue fell, losses persisted, and clinical trials for four PCR tests remain on track.CODX
Q2 202523 Nov 2025
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