Welcome to our dedicated page for Oncotelic Therapeutics news (Ticker: OTLC), a resource for investors and traders seeking the latest updates and insights on Oncotelic Therapeutics stock.
Oncotelic Therapeutics, Inc. (OTCQB: OTLC) generates a diverse stream of news centered on oncology, rare pediatric cancers, RNA-based therapeutics, AI-driven discovery, and nanomedicine. As a clinical-stage biopharmaceutical company, it regularly reports on scientific publications, joint venture progress, platform launches, and financing developments that shape its pipeline and corporate strategy.
Investors and researchers following OTLC news will encounter updates on key assets such as OT-101, a TGFB2 antisense agent associated with rare pediatric designation for DIPG through joint venture GMP Bio, and Sapu003, an intravenous Deciparticle formulation of everolimus developed by 45% owned JV Sapu Nano. Press releases highlight biomarker frameworks for identifying tumors likely to respond to Sapu003, pharmacokinetic data showing reduced gastrointestinal accumulation compared with oral everolimus, and broader Deciparticle platform data demonstrating formulation of multiple hydrophobic drug classes.
Oncotelic’s news flow also covers its PDAOAI evidence-interrogation platform, including open access for researchers to a TGF-β knowledge corpus of more than 125,000 PubMed abstracts via a dedicated Discord channel. Additional announcements describe peer-reviewed publications on context-dependent biomarkers in liver and pancreatic cancer, sub-15 nm nanoparticles for drug delivery, and survival-associated biological axes such as TGFB2, DNMT3A, and GMPS.
From a corporate and capital markets perspective, OTLC news includes independent valuations of its joint venture GMP Bio pipeline, potential fair-value remeasurements under U.S. GAAP, and registration statements related to equity purchase and note agreements with institutional investors. Regularly reviewing this news page allows readers to track how scientific advances, joint venture activities, AI platforms, and financing structures intersect within Oncotelic’s evolving oncology and rare disease portfolio.
Oncotelic Therapeutics, Inc. (OTCQB:OTLC) has announced a significant finding in its analysis of SARS-CoV-2, identifying the open reading frame 8 (ORF8) as a critical factor in the evolution of Delta and Omicron variants. The study revealed that higher serum levels of ORF8 in COVID-19 patients correlate with increased fatality rates. The company aims to leverage this information to develop therapeutics and vaccines targeting ORF8 as the virus mutates further. This analysis indicates an urgent need for ongoing innovation in COVID-19 treatment strategies.
Oncotelic Therapeutics (OTCQB:OTLC) announced that Dr. Anthony Maida will present at the 2nd Annual TGF-β for Immuno-Oncology Drug Development Summit from January 25-27, 2022. The summit will showcase TGF-β inhibitors' potential in oncology and virology, particularly OT-101. This first-in-class anti-TGF-β RNA therapeutic has shown promise against relapsed cancer and is currently under evaluation for severe COVID-19 cases. Oncotelic aims to enhance treatment outcomes for cancer, emphasizing rare pediatric conditions.
Oncotelic Therapeutics (OTCQB:OTLC) has submitted a clinical study protocol to the US FDA for a Phase 2 trial (M201) of OT-101, its TGF-β inhibitor, combined with Anti-PD-1 (Pembrolizumab) for treating Malignant Pleural Mesothelioma (MPM). OT-101 is a first-in-class RNA therapeutic showing efficacy in cancer and has demonstrated activity against the SARS-CoV-2 virus. The trial aims to assess TGF-β inhibition's impact on various solid tumors while evaluating changes in the tumor microenvironment.
Oncotelic Therapeutics, Inc. (OTCQB: OTLC) released its Q3 2021 financial results, reporting a net loss of $1.6 million, down from $2.0 million in Q3 2020. Total operating expenses rose to $1.8 million, driven by a $0.3 million decline in R&D costs and a $0.5 million increase in general and administrative expenses. The company secured $1.5 million in debt financing for a joint venture with Golden Mountain Partners (GMP) to advance its product pipeline, including OT-101. The promising efficacy signals from OT-101 for COVID-19 treatment were highlighted, with a reduction in mortality rates during trials.
Oncotelic Therapeutics (OTCQB:OTLC) announced positive results from its COVID-19 trial (C001) for OT-101, a first-in-class anti-TGF-β therapeutic. The trial met its safety and efficacy endpoints, showing a 4.5% mortality rate for OT-101 compared to 20% for placebo. Additionally, it achieved a viral load knockdown of 89% versus 67% for placebo, and improved survival for critical patients from 4 days (placebo) to 14 days (OT-101). These results support the further development of OT-101 for severe respiratory infections, including COVID-19.
Oncotelic Therapeutics (OTCQB:OTLC) announced progress in its ongoing OT-101/IL-2 combination trial, successfully completing the safety evaluation phase. This advancement allows for expansion into Phase 2 clinical trials and increased dosage levels. OT-101 is a first-in-class TGF-β targeting therapeutic, showing promising safety and efficacy in patients with advanced solid tumors. The optimal dosage from prior trials is being explored further. Results from this trial could enhance cure rates for metastatic kidney cancer and melanoma.
Oncotelic Therapeutics (OTCQB:OTLC) provided an update on its Phase 2 C001 Covid Study and the OT-101-ONC program, focusing on TGF-β immunotherapy for oncology and virology. Data lock for the Covid study was completed, with top-line results pending data analysis. The OT-101-ONC program has expanded to target cancers like mesothelioma and pancreatic cancer, supported by partnerships with leading pharmaceutical companies. Ongoing clinical trials with IL-2 and PD-1 inhibitors are expected to advance in 2021-2022. Oncotelic aims to enhance treatment outcomes for cancer patients.
Oncotelic Therapeutics (OTLC) has signed an exclusive licensing agreement with Autotelic Inc. for the development of AL-101, an intranasal apomorphine treatment targeting Parkinson's Disease and Erectile Dysfunction. The company aims to leverage the 505(b)2 regulatory pathway to expedite AL-101's market entry, having completed six clinical trials involving over 200 patients. Given the rising incidence of Parkinson's and unmet needs in sexual dysfunction, the acquisition positions Oncotelic for significant growth in these markets.
Oncotelic Therapeutics (OTCQB:OTLC) has signed a binding term sheet with Autotelic Inc. to license AL-101, an intranasal apomorphine aimed at treating Parkinson Disease (PD), Erectile Dysfunction (ED), and Female Sexual Dysfunction (FSD). This product will utilize the fast-to-market 505(b)2 regulatory pathway. AL-101 has completed six clinical trials with over 200 patients, demonstrating safety and efficacy. The growing incidence of PD and ED highlights the potential market for AL-101, offering a new therapeutic alternative for treatment-resistant patients.
Oncotelic Therapeutics (OTCQB:OTLC) announced positive results from its ARTI-19 clinical trial assessing PulmoHeal/ArtiVeda for treating mild to moderate COVID-19. The study demonstrated significant efficacy, with the artemisinin+SOC group showing faster improvement in WHO severity scale scores and respiratory metrics compared to standard of care. No serious side effects were reported, and the treatment was well-tolerated. This promising data will support Oncotelic's regulatory submission for marketing approval. The company aims to expand PulmoHeal/ArtiVeda's market presence as phytomedicine.