Dr. Vuong Trieu, Developer of Novel Oncology and Immunotherapy Assets, Leads Oncotelic Therapeutics’ Commitment to Innovation, Life-Saving Therapies
Oncotelic Therapeutics (OTCQB: OTLC) highlighted the contributions of Chairman and CEO Dr. Vuong Trieu and provided an update on its clinical pipeline. Dr. Trieu, a renowned industry pioneer, has an extensive portfolio of over 500 filed patents and 75 issued patents covering various therapeutic areas.
His notable achievements include co-inventing Abraxane® (acquired for $2.9 billion) and developing Cynviloq™ (sold for $1.3 billion). The company's pipeline includes six key programs: OT-101 (Phase 3 for pancreatic cancer), OXi4503 (Phase 2 in AML/MDS), CA4P/Fosbretabulin, AL-101 (Phase 2 for Parkinson's), AL-102 (discovery stage), and pediatric rare disease programs.
Oncotelic Therapeutics (OTCQB: OTLC) ha messo in evidenza il ruolo del presidente e CEO, il dott. Vuong Trieu, fornendo un aggiornamento sul suo portafoglio clinico. Il dott. Trieu, pioniere riconosciuto nel settore, vanta un ampio patrimonio di oltre 500 domande di brevetto e 75 brevetti concessi in diversi ambiti terapeutici.
Tra i suoi successi figura la co‑invenzione di Abraxane® (ceduto per $2,9 miliardi) e lo sviluppo di Cynviloq™ (venduto per $1,3 miliardi). La pipeline dell’azienda comprende sei programmi chiave: OT-101 (Fase 3 per il cancro pancreatico), OXi4503 (Fase 2 in AML/MDS), CA4P/Fosbretabulin, AL-101 (Fase 2 per il morbo di Parkinson), AL-102 (fase di scoperta) e programmi per malattie rare pediatriche.
Oncotelic Therapeutics (OTCQB: OTLC) destacó las aportaciones del presidente y CEO, el Dr. Vuong Trieu, y ofreció una actualización de su cartera clínica. El Dr. Trieu, pionero reconocido en la industria, cuenta con un extenso historial de más de 500 solicitudes de patente y 75 patentes concedidas en diversas áreas terapéuticas.
Entre sus logros figura la co‑invención de Abraxane® (adquirido por $2,900 millones) y el desarrollo de Cynviloq™ (vendido por $1,300 millones). La cartera de la compañía incluye seis programas clave: OT-101 (Fase 3 para cáncer de páncreas), OXi4503 (Fase 2 en LMA/SMD), CA4P/Fosbretabulin, AL-101 (Fase 2 para Parkinson), AL-102 (etapa de descubrimiento) y programas para enfermedades raras pediátricas.
Oncotelic Therapeutics (OTCQB: OTLC)는 회장 겸 CEO인 Dr. Vuong Trieu의 기여를 강조하고 임상 파이프라인 업데이트를 발표했습니다. 업계의 저명한 개척자인 Dr. Trieu는 다양한 치료 분야를 포괄하는 500건 이상의 출원 특허와 75건의 등록 특허을 보유하고 있습니다.
그의 주요 성과로는 Abraxane®의 공동 발명(매각가 $29억)과 Cynviloq™ 개발(매각가 $13억)이 있습니다. 회사의 파이프라인은 6가지 핵심 프로그램을 포함합니다: OT-101(췌장암 3상), OXi4503(AML/MDS 2상), CA4P/Fosbretabulin, AL-101(파킨슨병 2상), AL-102(발견 단계), 소아 희귀질환 프로그램들.
Oncotelic Therapeutics (OTCQB: OTLC) a mis en avant les contributions du président‑directeur général, le Dr Vuong Trieu, et a publié une mise à jour de sa pipeline clinique. Le Dr Trieu, pionnier reconnu de l’industrie, possède un vaste portefeuille de plus de 500 demandes de brevet et 75 brevets délivrés couvrant divers domaines thérapeutiques.
Parmi ses réalisations figure la co‑invention d’Abraxane® (cédé pour 2,9 milliards $) et le développement de Cynviloq™ (vendu pour 1,3 milliard $). La pipeline de la société comprend six programmes clés : OT-101 (Phase 3 pour le cancer du pancréas), OXi4503 (Phase 2 en LMA/SMD), CA4P/Fosbretabulin, AL-101 (Phase 2 pour la maladie de Parkinson), AL-102 (stade découverte) et des programmes pédiatriques pour les maladies rares.
Oncotelic Therapeutics (OTCQB: OTLC) hob die Verdienste von Vorstandsvorsitzendem und CEO Dr. Vuong Trieu hervor und gab ein Update zur klinischen Pipeline. Dr. Trieu, ein anerkannter Branchenpionier, verfügt über ein umfangreiches Portfolio von mehr als 500 eingereichten Patenten und 75 erteilten Patenten in verschiedenen therapeutischen Bereichen.
Zu seinen bemerkenswerten Erfolgen zählen die Mitentwicklung von Abraxane® (veräußert für $2,9 Milliarden) und die Entwicklung von Cynviloq™ (verkauft für $1,3 Milliarden). Die Pipeline des Unternehmens umfasst sechs Schlüsselprogramme: OT-101 (Phase 3 bei Bauchspeicheldrüsenkrebs), OXi4503 (Phase 2 bei AML/MDS), CA4P/Fosbretabulin, AL-101 (Phase 2 für Parkinson), AL-102 (Entdeckungsphase) und pädiatrische Programme für seltene Erkrankungen.
- Extensive intellectual property portfolio with over 500 filed patents and 75 issued patents
- Strong track record of successful drug development and monetization (Abraxane® $2.9B, Cynviloq™ $1.3B)
- Diverse clinical pipeline with six programs across different development stages
- Focus on high-value areas including oncology, rare diseases, and neurology
- Multiple early-stage programs requiring significant development funding
- Trading on OTCQB market rather than major exchange
- High dependency on single executive (Dr. Trieu) for innovation and leadership
Dr. Trieu’s prolific career includes multibillion-dollar drug discoveries targeting cancers of the breast, pancreas and non-small cell lung cancer, among others
Oncotelic’s robust portfolio and clinical pipeline is supported by the innovations and intellectual property generated by Dr. Trieu
AGOURA HILLS, Calif., Sept. 04, 2025 (GLOBE NEWSWIRE) -- via IBN -- Oncotelic Therapeutics, Inc. (OTCQB: OTLC) (“OTLC” or the “Company”), a clinical stage biopharmaceutical company developing transformative oncology and immunotherapy treatments, today shares an update on its clinical pipeline and highlights the invaluable contributions of its Chairman and CEO Dr. Vuong Trieu, who is recognized worldwide for his extraordinary intellectual property portfolio and impact on the biopharma industry.
Dr. Trieu is a prolific industry pioneer with over 500 filed patents and 75 issued patents covering biologics, small molecules, nanoparticles, diagnostics. Over his career he has invented, co-invented, and developed multiple novel therapeutics that have advanced to U.S. Food and Drug Administration (FDA) approval or late-stage development. Most notably, Dr. Trieu co-invented and developed Abraxane® (nab-paclitaxel), acquired by Celgene in 2010 as part of a
OTLC Pipeline Overview
- OT-101 (TGF-β inhibitor): Phase 3 for pancreatic cancer, with additional applications in ARDS/COVID-19
- OXi4503 (vascular disrupting agent): Phase 2 in AML/MDS; advancing toward pivotal phase 3 design
- CA4P / Fosbretabulin: Late-stage oncology asset currently under repositioning
- AL-101 (intranasal apomorphine): Phase 2 for Parkinson’s disease and Sexual Dysfunctions
- AL-102 (oligonucleotide antisense via intrathecal injection): Discovery stage for Alzheimer’s disease
- Pediatric Rare Disease Programs: Targeting orphan indications with the potential to generate Priority Review Vouchers (PRVs)
Dr. Trieu’s innovations form the cornerstone of OTLC’s intellectual property portfolio, reinforcing the Company’s strategy of building value through differentiated biotechnology assets with strong competitive barriers.
“Our strength lies not only in OTLC’s clinical pipeline but also in the breadth of intellectual property generated over my career, converting deep tumour-microenvironment biology into globally protected, clinic-ready technologies that redefine how drugs are delivered, monitored, and personalised,” said Dr. Trieu. “We remain committed to transforming these innovations into life-saving therapies for patients and long-term value for shareholders.”
About Oncotelic Therapeutics
Oncotelic Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on the development of oncology and immunotherapy products. The Company’s mission is to address high-unmet-need cancers and rare pediatric indications with innovative, late-stage therapeutic candidates.
In addition to its directly owned and developed drug pipeline, Oncotelic benefits from the robust portfolio of inventions created by its CEO, Dr. Vuong Trieu, who has filed over 150 patent applications and holds 39 issued U.S. patents. Beyond its internal programs, the Company also licenses and co-develops select drug candidates through joint ventures. Currently, Oncotelic owns
For more information, please visit: www.oncotelic.com
Oncotelic Cautionary Note on Forward‑Looking Statements
This press release contains forward‑looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements in this release other than statements of historical fact are forward‑looking and are based on current expectations, estimates, and projections about our business and future plans. In some cases, you can identify forward‑looking statements by terms such as “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “project,” “forecast,” “potential,” “continue,” and similar expressions (including the negative of such terms).
Forward‑looking statements in this release include, without limitation: our plans, timelines, and priorities for the OT‑101 program in PDAC and other indications; potential biomarker‑driven development strategies; the advancement, scope, timing, and results of current or future preclinical and clinical studies; regulatory interactions and potential approvals; development or commercialization of any product candidates within the Oncotelic/GMP Bio/Sapu ecosystem; the utility of our PDAOAI platform; future financings, strategic transactions, and/or public offerings involving our joint ventures or affiliates; and other statements that are not historical facts. Actual results may differ materially from those indicated by such forward‑looking statements as a result of various important factors, including, but not limited to: the inherent uncertainties of drug discovery and development; our ability to enroll patients and complete studies on expected timelines; whether preclinical or early clinical findings (including biomarker associations) will be replicated in larger, controlled trials; regulatory developments in the United States and other jurisdictions; competitive developments; our ability to obtain or maintain intellectual property protection; our liquidity and access to capital; the performance of collaborators, suppliers, and manufacturers; and other risks described in our filings with the Securities and Exchange Commission (SEC), including the “Risk Factors” section of our most recent Form 10‑K and subsequent periodic reports.
Forward‑looking statements speak only as of the date of this press release, and we undertake no obligation to update or revise such statements, whether as a result of new information, future events, or otherwise, except as required by law.
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