Newsoara BioPharma Expands Global Rights to vTv’s PDE4 Inhibitor HPP737 in $135 Million Deal

Newsoara BioPharma Co., Ltd. and vTv Therapeutics LLC have expanded their strategic collaboration, with Newsoara securing global rights to HPP737, a novel phosphodiesterase-4 (PDE4) inhibitor in development for psoriasis. The expanded agreement, valued at up to USD 135 million including a USD 20 million upfront payment, builds on their 2018 Asia-Pacific partnership and positions Newsoara to commercialize the anti-inflammatory therapy worldwide.

Transaction Structure

ElementDetail
LicensorvTv Therapeutics LLC (US-based)
LicenseeNewsoara BioPharma Co., Ltd. (China)
AssetHPP737 – Selective PDE4 inhibitor
Prior RightsChina and Asia-Pacific (2018 agreement)
Expanded RightsGlobal (ex-Asia-Pacific now included)
Upfront PaymentUSD 20 million
Total ConsiderationUp to USD 135 million (milestones and royalties)
Target IndicationPsoriasis (with potential expansion to other inflammatory diseases)

Product Profile & Mechanism of Action

FeatureHPP737 SpecificationDifferentiation
TargetPhosphodiesterase-4 (PDE4)Well-validated anti-inflammatory target (apremilast precedent)
SelectivityPotent and selective PDE4 inhibitionReduced off-target effects vs. non-selective PDE inhibitors
Anti-Inflammatory MechanismIL-23 and TNF-α suppression (in vitro and in vivo)Dual cytokine inhibition; potential for superior efficacy
Preclinical ValidationTherapeutic activity in multiple animal inflammation modelsStrong translational rationale for human psoriasis

Strategic Evolution & Market Context

TimelineMilestoneStrategic Significance
2018Newsoara secures China/Asia-Pacific rightsInitial partnership; regional development focus
2026Global rights expansionNewsoara positions as worldwide commercialization partner; vTv monetizes asset with limited ex-US infrastructure
Development StagePreclinical/early clinical (psoriasis)Phase I/II initiation anticipated; competitive PDE4 landscape requires differentiation
  • Psoriasis Market Opportunity: Global market >$25 billion; oral therapies (apremilast, deucravacitinib) gaining share vs. injectable biologics; HPP737 IL-23/TNF-α dual mechanism offers potential best-in-class positioning
  • PDE4 Competitive Landscape: Apremilast (Amgen) first-in-class but limited efficacy; deucravacitinib (BMS) TYK2 inhibitor sets higher efficacy bar; HPP737 requires superior clinical data for differentiation
  • Newsoara Global Ambition: Expansion from regional to global rights reflects China biotech maturation and capital markets support for international commercialization

Development & Commercial Outlook

PhaseActivityTimeline
CurrentGlobal rights transition; regulatory strategy alignmentQ1 2026
ClinicalPhase I/II psoriasis trial initiation2026-2027
ExpansionProof-of-concept in psoriatic arthritis, atopic dermatitis2027-2028
Global PartnershipUS/EU co-development or licensing discussionsData-dependent
CommercialChina launch (retained rights); ex-China partnership or self-commercialization2029+

Forward‑Looking Statements
This brief contains forward‑looking statements regarding HPP737 clinical development timelines, psoriasis market penetration, and Newsoara BioPharma’s global commercialization strategy. Actual results may differ due to Phase I/II efficacy outcomes, competitive dynamics with apremilast and deucravacitinib, and partnership negotiation results for US/EU markets.-Fineline Info & Tech