Ryvu Therapeutics (RVU) Corporate presentation summary
Event summary combining transcript, slides, and related documents.
Corporate presentation summary
4 May, 2026Pipeline and clinical development
Lead asset romaciclib (RVU120), a first-in-class oral CDK8/19 inhibitor, is in Phase II for AML and myelofibrosis, with promising efficacy and safety data, including 43% CR/CRi in VEN-refractory AML and spleen volume reductions in MF.
RVU305, a best-in-class, brain-penetrant PRMT5 inhibitor, is advancing through IND-enabling studies, showing superior potency and efficacy in MTAP-deleted cancers and strong CNS penetration.
Dapolsertib, a dual PIM/FLT3 inhibitor, is in Phase II for DLBCL in partnership with Menarini, with additional opportunities in hematologic malignancies.
ONCO Prime platform is generating novel precision oncology targets, including synthetic lethal targets, with initial data in colorectal cancer and collaborations with BioNTech and Exelixis.
Novel ADC payloads and immunocytotoxic strategies are being developed, including STING-activating ADCs, with multiple first-in-class candidates advancing.
Clinical results and regulatory progress
Romaciclib demonstrated the ability to overcome VEN resistance in AML, with a favorable safety profile and no significant increase in myelosuppression.
In myelofibrosis, romaciclib showed clinically meaningful spleen volume reductions and symptom improvements, especially in patients with ASXL1 and CALR mutations.
FDA Type C meeting in January 2026 provided guidance for U.S. expansion of romaciclib trials, with pivotal studies planned for 2026 and potential approval as early as 2028.
Medulloblastoma Phase I study in children is fully financed and set to start in 2026, with strong preclinical rationale and parallel U.S. study in preparation.
Market opportunity and financials
High unmet need in AML and MF, with global AML and MF markets projected to reach $6.6B and $2.9B by 2031, respectively.
Romaciclib positioned to set a new standard of care in post-VEN AML and post-JAKI MF, with strong commercial potential.
2025 revenues were €20.7M, with €14.7M from partnerships and €6.0M from grants; cash position as of March 2026 was €20.7M, plus €20.9M in non-dilutive grant funding.
Key partnerships with BioNTech and Exelixis have brought significant upfront payments, research funding, and milestone opportunities exceeding €50M and $400M, respectively.
Latest events from Ryvu Therapeutics
- Romaciclib delivers promising results in AML and MF, with a robust pipeline and strong partnerships.RVU
Corporate presentation19 Mar 2026 - Phase II trials show early efficacy and safety, with key data expected in Q1 and Q2 2025.RVU
Study Update11 Jan 2026 - Revenue fell and losses increased, but pipeline progress and new funding support future prospects.RVU
Q3 202520 Nov 2025 - Revenue up, net loss widened; cash runway extended to H2 2026 after reorganization.RVU
Q4 202417 Nov 2025 - Net loss widened on lower R&D revenue and NodThera revaluation; cash runway extended to H2 2026.RVU
Q2 202518 Sep 2025 - Operating revenue and cash rose, but net loss widened as clinical pipeline advanced.RVU
Q3 202413 Jun 2025 - Revenue up 43% year-over-year, net loss widens, pipeline and cash position strengthened.RVU
H1 202413 Jun 2025 - Ryvu drives innovation in oncology with first-in-class therapies and global clinical programs.RVU
Corporate Presentation13 Jun 2025 - Advancing first-in-class oncology therapies, Ryvu targets major hematology markets with global ambitions.RVU
Corporate Presentation13 Jun 2025