All prompts
Analyze
Audit a technology license clause by clause
Works the field, exclusivity, royalty base, diligence, improvements, sublicensing and termination clauses from your side of the table and hands back quoted language, paste-ready redlines, a fallback for each, and the order to push them in.
Your prompt
2
Pressure-test it
3
Go deeper
Before you run it
What to gather first
Watch for
What comes back
See an example of what you’ll get
*(After you answer the four questions: Northshore forecasts $180M peak sales starting 2031, Helix has two other interested licensees, only the upfront is agreed, and the vector was developed partly under an NIH grant.)*
Bottom line. Three issues from Helix's side: the field is broad enough to swallow the hematologic license Helix has already promised elsewhere; the sublicense clause gives Northshore consent-free rights and zero revenue share; and the royalty is a flat 4% with no minimums against a $180M forecast. Push field first while Helix still has two alternatives, then sublicense economics, then the escalator. Walk away on field breadth and sublicense share.
Field of use *(lead clause)*
- *As drafted, § 1.12:* "'Field' means therapeutic uses in oncology."
- *Analysis, licensor side:* Oncology covers solid tumors and hematologic malignancies. Helix's business plan reserves hematologic for a separate license to Riverpoint. As drafted, this grant forecloses that deal and Helix has no reservation clause to fall back on.
- *Redline:* "'Field' means therapeutic uses in solid tumors. All other indications, including hematologic malignancies, are expressly reserved to Licensor."
- *Fallback:* Solid tumors plus a 24-month right of first negotiation on hematologic, exercisable on payment of a $1.5M option fee.
Royalty base
- *As drafted, § 1.19:* "'Net Sales' means gross sales less reasonable deductions."
- *Analysis:* "Reasonable" is an open list: the licensee defines it annually and Helix audits after the fact. Combination products are unaddressed entirely, which matters because the vector will likely be sold with a companion agent.
- *Redline:* Closed list: actual returns and recalls; sales taxes and duties; separately stated freight and insurance; trade and quantity discounts actually allowed; chargebacks and rebates to government payors. Combination products allocated as A/(A+B) using average separate list prices in the same country, with Licensed Product never allocated below 50% of combination Net Sales.
- *Fallback:* Same closed list, combination floor at 40%.
Diligence
- *As drafted, § 4.1:* "Licensee will use commercially reasonable efforts to develop and commercialize."
- *Analysis:* Unenforceable as written. With exclusivity granted and no milestone, Northshore can hold the asset while it develops its internal program.
- *Redline:* IND filing within 18 months; first patient dosed within 36; pivotal start within 60; BLA within 84. Any miss, subject to a 6-month cure, lets Licensor convert the grant to non-exclusive or terminate.
- *Fallback:* Same milestones, 9-month cure, conversion only.
Sublicensing
- *As drafted, § 2.4:* "Licensee may sublicense without Licensor's consent and may retain all sublicense income."
- *Analysis:* Both halves are wrong for Helix. No consent means Helix could end up in business with a party it rejected; zero share hands away the upside on the most likely exit path for this asset.
- *Redline:* Consent not to be unreasonably withheld; sublicense income share of 30% pre-IND, 25% pre-pivotal, 20% thereafter; sublicenses consistent with this Agreement and terminable with it, subject to Licensor's election to recognize a compliant sublicensee directly.
- *Fallback:* Notice rather than consent, with 25/20/15 splits and the direct-recognition mechanic intact.
Encumbrance flag. If any of the vector work was NIH-funded, Bayh-Dole obligations attach: government license, US manufacturing preference, and march-in exposure. None of that appears in the draft. Helix cannot grant a clean worldwide exclusive until the funding history is confirmed. [UNVERIFIED - pull the grant records and any institutional patent agreement before the next call.]
Economics.
| Component | As drafted | Typical range | Helix ask | Fallback |
|---|---|---|---|---|
| Upfront | $4M | [UNVERIFIED - confirm comparables] | agreed, no change | n/a |
| Royalty | 4% flat | [UNVERIFIED] | 5 / 7 / 9 tiered at $250M and $1B | 5 / 6 / 7.5 |
| Minimums | none | [UNVERIFIED] | $5M from year 2 of sales | $3M |
| Sublicense share | 0% | [UNVERIFIED] | 30 / 25 / 20 | 25 / 20 / 15 |
Sequence. Field, then sublicense consent and share, then the royalty escalator and minimums, then the net-sales list. Field goes first because Helix's leverage is highest while two other licensees are live and the cost to Northshore of narrowing is lowest today.
Walk-away. Oncology-wide field with no reservation. Consent-free sublicensing with no revenue share. Any structure where Northshore can hold exclusivity with no milestone attached.
What your answers changed. The NIH answer and the two-live-licensees answer moved the most. Partial NIH funding is the entire Encumbrance flag. Without it there is no Bayh-Dole section, and I would have let Helix offer a clean worldwide exclusive it may not be able to grant. That two other licensees are live is why the push order opens on field rather than sublicense economics; if Northshore were the only party at the table, field goes last and becomes the thing I trade for the 30/25/20 sublicense split, because narrowing a field is the ask a licensee resists hardest once it knows it is the only bidder. The $180M forecast set the minimums and nothing else: $5M from year 2 of sales, $3M fallback, both priced off that number; at a $15M peak those figures are unaskable and the minimums row stays at none. Your "only the upfront is agreed" answer changed nothing: no ask on this list touches the $4M, so it confirmed what was in scope without moving a single number.
Why this prompt is built the way it is
## Framework
1. **Grant plus field is the economic perimeter.** Clarity beats breadth. "Therapeutic use in solid tumors" is a boundary; "biomedical applications" is a future dispute.
2. **Exclusivity is layered.** Exclusive even of the licensor, sole, or non-exclusive; within a field or across fields; geography; rights of first negotiation on adjacent fields.
3. **Base before rate.** The net-sales definition moves more money than the percentage. Open-ended deductions and unallocated combination products are where value leaks.
4. **Diligence with teeth or the exclusive is a shelf.** Each milestone needs an event, a date, and a consequence.
5. **Improvements come in four buckets**: licensor, licensee, joint, independent. Watch for a "derivative" definition that swallows the core IP.
6. **Sublicensing is an economics clause, not an administrative one.** Consent or notice, revenue share by stage, pass-through obligations, and what happens to sublicensees on termination.
7. **Audit rights need a threshold.** Frequency, scope, records retention, and who pays when the shortfall crosses the line.
8. **Termination is only half the clause.** Survival is the other half: sublicensees, accrued payments, confidentiality, grant-backs.
9. **Every criticism ships with a number.** Not "too narrow": the replacement language and the fallback you would sign.