Book a demo

Cut patent&paper research from weeks to hours with PatSnap Eureka AI!

Try now
Promega v. Aobious: NanoLuc Luciferase Substrate Patent Infringement | PatSnap
Explore in Eureka
Case ID1:25-cv-00244
FiledMar 2025
ClosedJul 2025
Patent Litigation

Promega v. Aobious: Consent Judgment & Permanent Injunction in NanoLuc Substrate Dispute

Promega Corporation secured a consent judgment and permanent injunction against Aobious Inc. in the Delaware District Court, finding infringement of four patents covering furimazine, hydrofurimazine, and fluorofurimazine luciferase substrates central to the Nano-Glo® product platform. The case resolved in just 134 days from filing — a signal of early settlement pressure and strong patent position.

Resolution time
134days
134 days from filing to consent judgment — well below the median D. Del. patent case duration
Patents asserted
4
US8809529, US10000500, US10669280 & US11691976 — furimazine-based NanoLuc luciferase substrates
Outcome
Consent Judgment
Court-entered judgment by agreement; infringement found, permanent injunction granted against Aobious
Cost ruling
Own Costs
Each party bears its own costs and attorneys’ fees under the consent judgment terms
Published by PatSnap Insights Team · Verified by PatSnap Eureka Data
Case overview

Promega locks down NanoLuc substrate IP with swift consent judgment

On 3 March 2025, Promega Corporation filed suit in the Delaware District Court against Aobious Inc., asserting infringement of four US patents — US8,809,529, US10,000,500, US10,669,280, and US11,691,976 — all directed to furimazine, hydrofurimazine, and fluorofurimazine compounds used as bioluminescent substrates in Promega’s proprietary NanoLuc® luciferase system. The complaint identified over 50 Aobious product listings spanning Nano-Glo® luciferase assay kits, HiBiT detection systems, NanoBRET® substrates, and in vivo fluorofurimazine reagents.

The case concluded on 15 July 2025 — just 134 days after filing — through a consent judgment signed by Judge Jennifer Choe-Groves. The judgment formally finds Aobious liable for infringement of all four asserted patents, enters a permanent injunction prohibiting Aobious from manufacturing, marketing, using, offering for sale, selling, or importing furimazine, hydrofurimazine, and fluorofurimazine products, and requires Aobious to make monetary payments to Promega per an undisclosed settlement agreement. No appeal rights were reserved by either party.

The 134-day resolution timeline is notably rapid even for consent judgments, suggesting Aobious was unable or unwilling to mount a substantive defence against Promega’s patent portfolio. The absence of defendant’s legal representation on the docket is consistent with an early capitulation or pre-litigation negotiation that converted to a formal court order. The specific monetary terms remain confidential within the settlement agreement, and the public record does not disclose any royalty rates or lump-sum figures agreed upon by the parties.

Case at a glance
Case no.1:25-cv-00244
DefendantAobious Inc.
CourtDelaware
JudgeJennifer Choe-Groves
FiledMarch 3, 2025
ClosedJuly 15, 2025
Duration134 days
OutcomeConsent Judgment
Verdict causeInfringement Action
BasisConsent Judgment
Prior Art Intelligence
See what prior art exists on this patent.
Eureka scans millions of patents and papers to surface prior art that may have invalidated these claims before costly litigation begins.
Check Prior Art
Case data sourced from PACER / Delaware District Court via PatSnap Eureka Litigation Intelligence Explore similar cases ↗
Case timeline

Filing to Consent Judgment in 134 days

134 days from filing to consent judgment — well below the median D. Del. patent case duration

Case timeline: Complaint filed MAR 3 2025, MAY–JUN — 134 days total Horizontal timeline showing the three key events in Promega Corporation v Aobious Inc. from filing to resolution. Source: PACER, Delaware District Court. MAR 3 2025 Complaint filed Pre-trial proceedings JUL 15 2025 Consent Judgment 134 DAYS TOTAL
Dismissal terms

Consent judgment entered: what the permanent injunction means for both parties

Legal mechanism

Consent judgment is a court-enforceable settlement

A consent judgment combines a negotiated settlement with judicial authority. Unlike a private settlement, it is entered as a court order, meaning Aobious’s compliance obligations are directly enforceable through contempt proceedings. The court explicitly retained jurisdiction for enforcement purposes. No appeal is permitted under the agreed terms, making the outcome final and immediately binding.

Judicially enforceable outcome
Plaintiff outcome

Promega secures permanent injunction across all furimazine variants

Promega obtained the strongest available civil remedy: a permanent injunction blocking Aobious from any commercial activity involving furimazine, hydrofurimazine, and fluorofurimazine products. Combined with an undisclosed monetary payment, this outcome validates Promega’s four-patent portfolio and removes a competing supplier from the market. The consent judgment also forecloses future re-entry by Aobious under the same product lines.

Injunction + monetary relief
Defendant outcome

Aobious exits the furimazine substrate market permanently

Aobious conceded infringement across all four asserted patents without mounting a recorded defence. The permanent injunction bars the company from the full commercial lifecycle — manufacture, marketing, sale, offer for sale, and importation — of the named substrate categories. The monetary obligation, while undisclosed, adds financial consequence to the operational shutdown. The no-appeal clause eliminates any future challenge pathway.

Full market exit required
Commercial implications

Promega’s NanoLuc substrate moat is reinforced

The consent judgment signals that Promega’s four-patent cluster covering furimazine-class substrates presents a formidable barrier to third-party suppliers of NanoLuc-compatible reagents. Any life science distributor supplying furimazine, hydrofurimazine, or fluorofurimazine without a Promega licence faces material litigation risk. Research procurement teams and reagent OEMs should conduct FTO analysis before sourcing or distributing these substrate classes.

High licence barrier for competitors
Legal analysis based on PACER docket records for case 1:25-cv-00244 and PatSnap Eureka litigation intelligence Search PatSnap Eureka ↗
Parties and representation

Full party and counsel information

RoleNameTypeDetail
PlaintiffPromega CorporationCompanyLife science reagent company — holder of US8809529, US10000500, US10669280 & US11691976Search in Eureka ↗
DefendantAobious Inc.CompanyAobious Inc. — distributor of research-use furimazine and luciferase substrate productsSearch in Eureka ↗
Plaintiff counselAndrew Mark MoshosAttorneyCounsel for Promega CorporationSearch in Eureka ↗
Plaintiff counselAnne M. ReynoldsAttorneyCounsel for Promega CorporationSearch in Eureka ↗
Plaintiff counselBindu Ann George PalapuraAttorneyCounsel for Promega CorporationSearch in Eureka ↗
Plaintiff counselDavid A. CasimirAttorneyCounsel for Promega CorporationSearch in Eureka ↗
Plaintiff counselDavid Ellis MooreAttorneyCounsel for Promega CorporationSearch in Eureka ↗
Plaintiff counselDavid W. StapleAttorneyCounsel for Promega CorporationSearch in Eureka ↗
Plaintiff counselMalisa DangAttorneyCounsel for Promega CorporationSearch in Eureka ↗
Plaintiff counselTyler E. CraggAttorneyCounsel for Promega CorporationSearch in Eureka ↗
Plaintiff law firmPotter Anderson & Corroon, LLPLaw FirmRepresenting Promega CorporationSearch in Eureka ↗
Presiding judgeJudge Jennifer Choe-GrovesJudgeDelaware District CourtSearch in Eureka ↗
Official verdict

Official order — verbatim text

“IT IS HEREBY FOUND, ORDERED, ADJUDGED, AND DECREED THAT: A. Promega Corporation’s (“Promega”) requests for a finding of infringement and an entry of a permanent injunction against Aobious Inc. (“Aobious”) is GRANTED. B. Aobious has infringed the United States Patent Nos. 8,809,529 (the “’529 Patent”), 10,000,500 (the “’500 Patent”), 10,669,280 (the “’280 Patent”), and 11,691,976 (the “’976 Patent” and collectively with the ’529 Patent, the ’280 Patent, and the ’500 Patent the “Asserted Patents”). C. A permanent injunction is hereby entered against Aobious. Aobious is permanently enjoined from the manufacture, marketing, use, offer for sale, sale, and/or importation of furimazine, hydrofurimazine, and fluorofurimazine products. D. Aobious shall make monetary payments to Promega as set out and defined in the settlement agreement entered into by and between the parties. E. This Court retains exclusive jurisdiction of this action for the purpose of ensuring compliance with this Consent Judgment and the settlement agreement. F. No appeal shall be taken by any party from this Consent Judgment. G. Except in the event of judicial enforcement of this Consent Judgment as outlined herein, each party shall bear its own costs and attorneys’ fees. H. This Consent Judgment shall finally conclude and dispose of all claims related to the Asserted Patents as to Promega and Aobious with respect to Aobious’s furimazine, hydrofurimazine, and fluorofurimazine products. I. This Consent Judgment shall be entered without further notice.”
Source: PACER Docket, Case 1:25-cv-00244, Delaware District Court

The consent judgment’s operative language — ‘IT IS HEREBY FOUND, ORDERED, ADJUDGED, AND DECREED’ — carries the same legal weight as a litigated judgment. By expressly finding infringement of all four asserted patents and entering a permanent injunction, the court created a judicially enforceable record that Aobious cannot later relitigate. The no-appeal clause, agreed by both parties, makes this disposition functionally final. The retained jurisdiction clause means any violation of the injunction terms exposes Aobious to contempt sanctions without a new lawsuit.

PACER case 1:25-cv-00244 · Public docket record Explore in Eureka ↗
Patent at issue

US8809529, US10000500, US10669280 & US11691976 — NanoLuc furimazine substrate patents

Publication No.US10669280B2
Application No.US16/545903
Patent details
ProductFurimazine coelenterazine-analogue substrates for NanoLuc luciferase bioluminescence assays
Cited in actionMarch 3, 2025

Publication No.US10000500B2
Application No.US15/661582
Patent details
ProductHydrofurimazine and coelenterazine-analogue substrate compositions for luciferase detection
Cited in actionMarch 3, 2025

Publication No.US8809529B2
Application No.US13/287992
Patent details
ProductFluorofurimazine and hydrofurimazine substrate compounds for bioluminescent reporter assays
Cited in actionMarch 3, 2025

Publication No.US11691976B2
Application No.US16/548214
Patent details
ProductFluorofurimazine in vivo bioluminescent substrate compositions and NanoLuc imaging methods
Cited in actionMarch 3, 2025

The four asserted patents collectively protect the chemical scaffold and use of furimazine-class coelenterazine analogues as substrates for the NanoLuc® small luciferase reporter system. US8,809,529, filed via application US13/287992, covers the foundational furimazine compound. US10,000,500 (US15/661582) and US10,669,280 (US16/545903) extend to hydrofurimazine variants and additional formulations. US11,691,976 (US16/548214) addresses fluorofurimazine, critical for in vivo imaging applications. Together they represent Promega’s layered IP strategy across the NanoLuc substrate chemistry space.

The NanoLuc platform has become a dominant bioluminescent reporter technology in drug discovery, protein interaction studies, and in vivo imaging. Furimazine and its derivatives are the essential consumable input — without a licence from Promega, third-party suppliers of these substrates face direct infringement exposure. The four-patent cluster, spanning applications filed from 2011 through 2019, provides overlapping coverage that makes substrate design-arounds technically and commercially challenging for any competitor seeking to serve this market segment.

Patent data sourced from USPTO via PatSnap Eureka patent database Search patent records in Eureka ↗
Freedom to operate

Should you run an FTO against US8809529, US10000500, US10669280 & US11691976?

Any company manufacturing, distributing, or importing furimazine, hydrofurimazine, or fluorofurimazine for research or commercial use should treat Promega’s four-patent cluster as a primary FTO target. The consent judgment in this case confirms Promega’s active enforcement posture. Life science reagent distributors, contract research organisations, and biopharma in vivo imaging teams sourcing NanoLuc-compatible substrates outside Promega’s authorised supply chain carry meaningful litigation exposure.

PatSnap Eureka’s FTO Search Agent can map your substrate chemistry and product specifications against the claim scope of US8,809,529, US10,000,500, US10,669,280, and US11,691,976 in minutes. Eureka’s patent landscape tools also identify design-around opportunities and flag any continuation or divisional applications in Promega’s NanoLuc portfolio that may extend protection beyond these four granted patents. Start your FTO analysis before product launch or procurement commitments.

PatSnap Eureka FTO Search

Run a freedom-to-operate analysis on US10669280B2 to assess your product’s exposure

Run FTO in Eureka →
Related litigation

Similar NanoLuc substrate and bioluminescence reagent patent cases

Cases involving furimazine-based luciferase substrate patents and bioluminescence reagent IP enforcement in US district courts, including Delaware.

🔍
Access 40+ similar cases in PatSnap Eureka
Promega Corporation patent enforcement history, Delaware case history, Promega Corporation’s full IP portfolio, and comparable case analysis
Promega v. other distributorsNanoLuc IP enforcement historyCoelenterazine analogue disputesD. Del. consent judgment timelines
Unlock similar cases in Eureka →
Strategic implications

What this case signals for the bioluminescence reagent IP landscape

Promega’s swift, injunction-backed victory illustrates the depth of its NanoLuc substrate patent estate and its willingness to enforce aggressively.

Four-patent cluster creates near-complete furimazine substrate coverage

Promega’s asserted patents span the original furimazine compound (US8,809,529) through hydro- and fluoro-variants (US10,000,500; US10,669,280; US11,691,976), suggesting a layered prosecution strategy designed to foreclose design-arounds. Any company working in NanoLuc-compatible substrate chemistry should map its product against all four patents before commercialisation.

Absence of defendant counsel signals early commercial capitulation

No defendant law firm appears on the docket, which is consistent with Aobious having accepted Promega’s terms before or shortly after filing. This pattern — immediate consent rather than inter partes review or invalidity counterclaims — suggests Promega’s patents were assessed as difficult to challenge on validity or that commercial exposure made litigation uneconomical for Aobious.

🔒
Full strategic analysis in PatSnap Eureka
Unlock deeper analysis of Promega’s bioluminescence substrate enforcement strategy and district court consent judgment risk factors.
Furimazine FTO risk mapNanoLuc licence benchmarksPromega enforcement pattern
Unlock full analysis →
Analysis powered by PatSnap Eureka Litigation Intelligence Explore in Eureka ↗
Frequently asked questions

Promega v Aobious — key questions answered

Still have questions? PatSnap Eureka can answer them instantly from patent and litigation data. Ask Eureka ↗
PatSnap Eureka

Protect your position in the bioluminescent substrate market

Promega’s consent judgment win confirms active enforcement of its NanoLuc substrate IP. Run an FTO against the four asserted patents and monitor Promega’s continuation filings with PatSnap Eureka before launching or distributing furimazine-class reagents.

Ask anything about this case.
PatSnap Eureka searches patents and litigation data to answer instantly.
Powered by PatSnap Eureka
Link copied to clipboard

Related Litigation Cases

Help us improve this page

Found incorrect or outdated information? Let us know and we'll get it fixed.