Precision Biosciences IncDTIL
Price$6.33Intrinsic value$11.3780% above price

Qualitative Analysis

Business overview

Business Overview

Precision BioSciences, Inc. (NASDAQ: DTIL) is a clinical-stage gene editing company headquartered in Durham, North Carolina. The company is dedicated to developing in vivo gene editing therapies using its wholly proprietary ARCUS genome editing platform. ARCUS is a highly specific and versatile platform based on a naturally occurring genome editing enzyme, I-CreI, which allows for precise DNA insertions (knock-ins), deletions (knock-outs), and repairs. ARCUS's relatively small size compared to CRISPR-Cas9 simplifies delivery to target tissues using viral and non-viral methods. Precision's primary clinical focus is on advancing its wholly owned programs, including PBGENE-HBV for chronic hepatitis B and PBGENE-DMD for Duchenne muscular dystrophy.

Research as of 19 Jun 2026

Strategic Initiatives

Growth programs, investments, and their expected impact

AI-assisted
In Vivo Gene Editing PivotTransformation

Precision BioSciences has strategically pivoted to focus exclusively on in vivo gene editing therapies utilizing its proprietary ARCUS platform, while out-licensing its ex vivo CAR T assets to partners to reduce operating spend and extend cash runway.

Expected impact: Extends cash runway through 2028 and concentrates scientific focus on high-value in vivo programs like PBGENE-HBV and PBGENE-DMD.

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InvestmentPrioritized allocation of R&D resources, offset by an estimated $20 million reduction in annual operating spend from the CAR T infrastructure transfer.
TimelineInitiated in August 2023 with the Imugene transaction; ongoing execution through 2026-2028.
PBGENE-HBV Clinical Development (ELIMINATE-B)Innovation

Advancing the first-in-human Phase 1/2a ELIMINATE-B clinical trial evaluating PBGENE-HBV, a novel in vivo gene editing therapy designed to eliminate cccDNA and inactivate integrated HBV DNA to achieve a functional cure for chronic Hepatitis B.

Expected impact: Establish clinical proof of concept for ARCUS-based viral DNA elimination and transition the trial into Part 2 expansion.

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InvestmentCore clinical R&D funding supported by the company's cash reserves.
TimelineOngoing clinical trial; expanded into France and Romania in early 2026; additional updates expected by the end of 2026.
PBGENE-DMD Clinical Initiation (FUNCTION-DMD)Innovation

Initiating the Phase 1/2 FUNCTION-DMD clinical trial for PBGENE-DMD, an in vivo gene editing candidate utilizing a gene excision approach to restore a near-full length functional dystrophin protein in patients with Duchenne muscular dystrophy.

Expected impact: Demonstrate safety, tolerability, and dystrophin protein expression in ambulatory DMD patients.

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InvestmentCore clinical R&D funding; program has received FDA Fast Track, Rare Pediatric Disease, and Orphan Drug designations.
TimelineIND cleared in Q1 2026; first clinical site activated in April 2026; patient dosing and initial data expected in 2026.
Sources: 2

Mergers, Acquisitions & Partnerships

Recent deals and strategic collaborations

AI-assisted

Strategic Partnerships

TG TherapeuticsOut-licensing and Development Agreement

Grants TG Therapeutics exclusive worldwide rights to develop and commercialize azer-cel (Azercabtagene Zapreleucel) for autoimmune diseases and other non-oncology indications, allowing Precision to monetize its CAR T technology while focusing on in vivo programs.

Terms: Precision received upfront and near-term payments, including a $7.5 million milestone payment in April 2026 (consisting of $5.25 million cash and $2.25 million equity investment). Precision remains eligible for further development, regulatory, and commercial milestones, plus royalties on net sales.

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Imugene LimitedOut-licensing and Infrastructure Transaction

Imugene assumed global rights to azer-cel for cancer indications and took over Precision's cell therapy manufacturing infrastructure and clinical team, significantly reducing Precision's operating expenses.

Terms: Upfront economics valued at $21 million in cash and equity, plus an $8 million milestone payment received in Q4 2025. Precision is eligible for up to $198 million in additional milestones and double-digit royalties on net sales.

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iECUREResearch and Development Collaboration

Collaboration utilizing Precision's ARCUS platform for a gene insertion approach to treat neonatal-onset ornithine transcarbamylase (OTC) deficiency.

Terms: Precision is eligible for milestone payments and royalties on future product sales as iECURE advances the candidate (ECUR-506).

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Sources: 1
AI-assisted, source-linked narrative; figures from company filings (SEC EDGAR) and market data. Dates shown per section. Not investment advice. Terms of Use.