Confidential Teaser Memorandum · June 2026

A Precisely Timed Entry into the IBS Market

GreenSpace Labs is seeking a licensing or co-development partner to advance a Phase 2 cannabinoid asset ahead of the most significant concurrent branded patent cliff in IBS history.

Clinical Stage

Phase 2

Proof-of-Concept Complete


GSL-01-001

Lead Program

2028–29

Target Window

Opportunity Snapshot

The Market. The Moment. The Asset.

A clinical-stage cannabinoid program positioned at the intersection of a $3.6B market, a 13-month generic dislocation window, and a validated regulatory pathway.

$3.6B

Global IBS Market (2024) ~9% CAGR to ~$6B by 2030

13 mo.

LOE Cliff Window Jun 2028 – Mar 2029

Phase 2

GSL Clinical Stage Proof-of-Concept Complete

$250M+

Conservative Yr-3 Revenue 5–10% IBS-D/pain share

Between June 2028 and March 2029, three of the four leading branded IBS products face settled generic launches — creating a finite window for a differentiated entrant.

The Window

Three Category Leaders. One 13-Month Window.

Viberzi, Xifaxan, and Linzess face generic launches within 13 months of each other. Branded promotional spend collapses. Payer formulary tiers reset. ~14,000 US gastroenterologists actively re-evaluate their prescribing.

HighIBS-D

Xifaxan

Bausch Health


Generic Launch

June 2028

SevereIBS-D

Viberzi

AbbVie


Generic Launch

July 2028

HighIBS-C

Linzess

AbbVie / Ironwood


Generic Launch

March 2029

A mechanism-distinct branded entrant is not displaced by generic eluxadoline, rifaximin, or linaclotide — it captures the differentiation premium those brands forfeit.

The Asset

GSL-01-001 — Multi-Pathway Cannabinoid Formulation

  • Program:GSL-01-001 — proprietary cannabinoid formulation (oral)
  • Stage:Phase 2 pilot complete; proof-of-concept data available
  • Indication:IBS — all subtypes; primary focus on abdominal pain and IBS-D
  • Mechanism:Multi-pathway cannabinoid pharmacology targeting visceral pain, motility, and gut-brain signaling
  • Differentiation:Mechanism-distinct from all three LOE products; addresses pain directly vs. downstream bowel-habit normalization
  • IP:Proprietary formulation; composition and method claims in development

Phase 2 Highlight

51% → 10%

Patients reporting severely impacted QoL, baseline to Week 8


IBS-QoL data: patients reporting 'quite a bit' or 'extremely' impacted quality of life declined from 51% at baseline to 10% by Week 8 (n=23, 12-week treatment).

n=2312-weekPhase 2 Pilot

Lessons from Olorinab

Designed to Solve the Prior Failure

The most significant prior cannabinoid IBS program failed. GSL's formulation is specifically designed to address those failure modes.

Prior Failure

Prior Failure: Olorinab (APD371)

Selective CB2 agonist acquired by Pfizer/Arena ($6.7B, 2021) — failed in CAPTIVATE Phase 2b.

Prior Failure

Failure Mode

Single-mechanism, single-receptor agonism proved insufficient in a multifactorial disease with robust placebo response.

GSL Approach

GSL's Approach

Multi-pathway engagement designed to address these failure modes directly — engaging multiple cannabinoid pathways rather than a single receptor target.

GSL Approach

Validated Regulatory Pathway

Epidiolex (Jazz/GW Pharma, $7.2B) and Sativex confirm cannabinoid Rx infrastructure exists. The indication-mechanism fit in IBS requires the multi-pathway approach.

2027–2032

The Window to Capture Dislocation is Finite

$250M–$500M

Conservative annual revenue by Year 3

5–10% IBS-D/pain share on $5B+ addressable market

Multi-Indication

Franchise Runway

IBD-associated pain, functional dyspepsia, post-infectious GI pain syndromes

2031+

= Commoditized Field

Programs arriving after the cliff inherit a generic-dominated landscape

Partnership Rationale

Seeking a Mid- to Large-Cap Pharma Partner

Ideally an organization with existing cannabinoid Rx infrastructure or a GI franchise, capable of pivotal-stage execution and commercial launch by 2028–2029.

Request NDA & Data Package

Indicative Deal Parameters

Deal Structure

  • Structure: Exclusive worldwide license; co-development or full acquisition considered
  • Economics: Upfront license fee + development milestones + tiered royalties on net sales
  • Data Package: Phase 2 CSR, formulation IP, regulatory correspondence, preclinical package (under NDA)
  • Timeline: Partner targeting pivotal-stage initiation 2027; commercial launch aligned to 2028–2029 cliff

Contact

Richard D. Bailey | COO & CFO
GreenSpace Labs, Inc.
1151 Aquidneck Ave. #540, Middletown, RI 02842

[email protected]
GreenSpace LabsGreenSpace Labs

This teaser memorandum is confidential and intended solely for qualified recipients evaluating a potential business relationship with GreenSpace Labs, Inc. It does not constitute an offer to sell or a solicitation to buy any security. Market data sourced from public filings, peer-reviewed literature, and industry sources as of May 2026.

© 2026 GreenSpace Labs, Inc. All rights reserved.[email protected]