No real transactions

Liquidity planner

Model external funding, pool execution and operating requirements. Founder contribution: $0. This page accepts no funds.

Funding assumptions

Scenario inputs only. The reserve is an assumption; actual bonds and operating costs need verification. Deployment gas also requires an ETH sponsor.

Saves JSON to your device. No submission, pledge or wallet transaction.
  • LP capital bears inventory risk; informed trading can outweigh collected fees.
  • A funding cohort needs declared activation, expiry, refund, custody and allocation terms before accepting deposits.
  • Gas, oracle bonds, disputes and review require separately identified funding even with $0 founder contribution.

Execution model

A neutral 50¢ opening inventory price and the native 50-bps smaller-leg fee fixture are used here. These are illustrations, not clinical probabilities or approved live terms.

Outcome tokens
197.08
Average execution price
50.74¢
Cost above opening marginal price
1.48%
Marginal price after trade
50.99¢
Assumed trading fee
50 bps smaller leg / $0.49

Native integer constant-product illustration; fees stay outside reserves. Excludes gas, oracle costs and other trades. No APY, return guarantee, token subsidy or leverage is assumed.

Before a market opens

Reviewed event
An exact application or clinical condition, source hierarchy, cutoff and YES / NO / INVALID terms.
Funded exposure
Opposing traders can fund pairs. A seeded AMM needs LP capital, risk limits and separately funded gas, bonds and monitoring.
Tested settlement
Commit the rules and rehearse disputes, final settlement and holder redemption under the reviewed configuration.

Research candidates

October 28, 2026 source snapshot. These are unlisted candidates with $0 committed. Rank reflects editorial suitability, not measured demand; status and final rules need review.

NTLA

lonvoguran ziclumeran (lonvo-z)

Intellia Therapeutics · hereditary angioedema

Research note & open risks

In vivo CRISPR regulatory milestone; recognizable gene-editing theme. Demand is a hypothesis, not measured.

Novel modality raises safety and interpretation risk; exact approved population must be pinned.

BLTE

tinlarebant

Belite Bio · Stargardt disease type 1

Research note & open risks

Single named rare-eye-disease NDA; accessible binary regulatory question.

Pin age range, indication and approval definition; do not confuse US decision with Japanese or Access Consortium submissions.

DYN

zeleciment rostudirsen (z-rostudirsen / DYNE-251)

Dyne Therapeutics · Duchenne muscular dystrophy amenable to exon 51 skipping

Research note & open risks

Priority-reviewed DMD BLA with an explicit target; catalyst soon enough to test retention.

Accelerated approval based on surrogate endpoint needs explicit treatment; skip if safe release cannot precede target with useful lead time.

AXSM

AXS-12 (reboxetine)

Axsome Therapeutics · cataplexy in narcolepsy

Research note & open risks

Specific CNS NDA with long preparation runway; substitute for DYN if launch slips.

Longer capital lock-up; approval of another Axsome product cannot satisfy this question.

BBIO

encaleret

BridgeBio Pharma · autosomal dominant hypocalcemia type 1 (ADH1)

Research note & open risks

Genetic-disease franchise and clear NDA target; differentiated from first basket.

Issuer has multiple regulatory programs; May 8 date is encaleret, not oral infigratinib or BBP-418.

EXEL

zanzalintinib in combination with atezolizumab

Exelixis · metastatic colorectal cancer

Research note & open risks

Oncology catalyst with public extension history; useful independent regulatory category.

Old December 3 2026 date is superseded; combination and treatment line must match final resolution text.

PHVS

deucrictibant immediate-release 20mg

Pharvaris · on-demand treatment of hereditary angioedema attacks

Research note & open risks

Oral HAE treatment is explainable to traders; useful later comparable to gene editing.

HAE economic theme overlaps NTLA; avoid correlated concentration and do not confuse IR with XR prophylaxis.

INBX

ozekibart (INBRX-109)

Inhibrx Biosciences · unresectable or metastatic conventional chondrosarcoma

Research note & open risks

Named BLA in rare oncology indication with an explicit target.

Distinguish conventional histology and disease stage; review updated safety and any changed FDA timetable before publication.

UNCY

oxylanthanum carbonate

Unicycive Therapeutics · hyperphosphatemia in chronic kidney disease patients on dialysis

Research note & open risks

Fresh NDA resubmission target; manufacturing-versus-efficacy distinction can support research content.

Prior CRLs and third-party manufacturing inspections make timing discontinuous; target may accelerate or slip.

GILD

once-weekly oral Yeztugo (lenacapavir) 300mg tablet

Gilead Sciences · HIV pre-exposure prophylaxis

Research note & open risks

Broadly recognizable HIV-prevention franchise; diversifies small biotech concentration.

Existing twice-yearly injectable approval is not approval of this weekly oral formulation; ticker stock hedge is especially noisy.

These dates provide no official time or approved market resolution deadline.

Planning only. No release or capital allocation is approved through this page.