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Medicus Pharma Raises $11.2 Million to Advance Novel Microneedle Patch for Basal Cell Carcinoma Treatment

  • Medicus Pharma completed two public offerings totaling $11.2 million to fund Phase 2 clinical trials of its innovative doxorubicin-loaded dissolvable microneedle patch for basal cell carcinoma treatment.
  • The company's Phase 1 study demonstrated promising efficacy with six participants achieving complete response on histological examination, meeting primary safety and tolerability objectives.
  • Proceeds will support ongoing Phase 2 trials in the US and Europe, with potential expansion to pivotal studies and treatment of other non-melanoma skin diseases.
  • The novel D-MNA patch represents a non-invasive alternative to traditional surgical approaches for basal cell carcinoma, the most common form of skin cancer.

Robust Pipeline for Nasopharyngeal Cancer Treatment Emerges with 25+ Pharmaceutical Companies Developing Novel Therapies

  • A comprehensive pipeline analysis reveals over 25 pharmaceutical companies actively developing approximately 30 drug candidates for nasopharyngeal cancer, signaling significant industry investment in this therapeutic area.
  • BL-B01D1, a first-in-class bispecific antibody-drug conjugate targeting both EGFR and HER3, has advanced to Phase III clinical trials, showing promise for patients with recurrent or metastatic nasopharyngeal carcinoma.
  • Novel approaches in development include Takeda's TAK-500, a STING agonist immunostimulatory antibody drug conjugate, and Ascentage Pharma's APG-5918, highlighting diverse therapeutic strategies targeting this challenging cancer.

Biopharma M&A Activity Reaches $79.4 Billion in 2024 Despite 50% Drop from Previous Year

  • Biopharma M&A activity totaled $79.4 billion in 2024, representing approximately half of 2023's total value, though deal volume saw a slight increase when excluding four mega-deals from the previous year.
  • Vertex Pharmaceuticals led the year's largest acquisition with its $4.9 billion purchase of Alpine Immune Sciences, followed by Gilead's $4.3 billion acquisition of CymaBay and Eli Lilly's $3.2 billion purchase of Morphic.
  • Oncology remained the dominant therapeutic area for dealmaking, accounting for more than a third of all 2024 biopharma transactions by both number and total value, with approximately $90 billion in cancer-focused deals.
  • Deal activity shifted toward earlier-stage assets and smaller transactions as buyers digested large previous acquisitions and the supply of late-stage and marketed assets diminished.

RedHill Biopharma Reports Strong Start to 2025 with Strategic Partnerships and Commercial Growth

  • RedHill Biopharma has out-licensed RHB-102 to Hyloris in a deal potentially worth up to $60 million plus royalties, strengthening their financial position and development capabilities.
  • The company has initiated a Bayer-funded Phase 2 clinical study of opaganib in combination with darolutamide for advanced prostate cancer, expanding their oncology portfolio.
  • Talicia®, RedHill's H. pylori treatment, has surpassed 100,000 prescriptions and secured Humana® Part D Plan coverage, adding access for over eight million Medicare beneficiaries without prior authorization requirements.

Zydus Lifesciences Partners with Synthon for Novel Cancer Drug Development in $1.5 Billion US Market

  • Zydus Lifesciences has signed an exclusive agreement with Netherlands-based Synthon BV for the development and commercialization of a novel 505(B)(2) oncology product targeting an undisclosed indication in the US market.
  • The partnership divides responsibilities with Synthon handling development, manufacturing and supply while Zydus manages NDA submission and commercialization, with filing expected in 2026.
  • The novel cancer drug is designed to offer additional strengths intended to reduce pill burden, provide flexibility for dose adjustments, and enhance patient compliance in a high unmet medical need area.
  • The addressable market size for the investigational drug's reference product is estimated at approximately $1.5 billion as of December 2024 according to IQVIA MAT data.

Targeted Therapies and Immunotherapy Advances in Non-Small Cell Lung Cancer: A Comprehensive Review

  • Targeted therapies for NSCLC have revolutionized treatment for patients with specific genetic alterations, with EGFR, ALK, and ROS1 inhibitors showing significant improvements in progression-free survival compared to traditional chemotherapy.
  • Immunotherapy, particularly immune checkpoint inhibitors targeting PD-1/PD-L1 and CTLA-4, has become a cornerstone in NSCLC treatment, with newer targets like LAG-3, TIM-3, and TIGIT showing promise in ongoing clinical trials.
  • Advanced cellular therapies including adoptive cell transfer, CAR-T cells, and cancer vaccines represent the next frontier in NSCLC treatment, particularly for patients with "cold tumors" who don't respond to standard immunotherapies.
NCT03729596TerminatedPhase 1
MacroGenics
Posted 11/21/2018
NCT05202561Unknown StatusPhase 1
First Affiliated Hospital Bengbu Medical College
Posted 3/10/2022
NCT01935154CompletedPhase 2
Vaxon Biotech
Posted 8/1/2012
NCT02587689Unknown StatusPhase 1
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
Posted 10/1/2015
NCT04646330CompletedPhase 1
Akeso
Posted 11/18/2020
NCT03789604Active, Not RecruitingPhase 3
CStone Pharmaceuticals
Posted 12/13/2018
NCT02349724Unknown StatusPhase 1
Southwest Hospital, China
Posted 12/1/2014
NCT03525782Unknown StatusPhase 1
The First Affiliated Hospital of Guangdong Pharmaceutical University
Posted 2/1/2018
NCT04908111SuspendedPhase 1
Cancer Research UK
Posted 10/15/2021
NCT02576574CompletedPhase 3
EMD Serono Research & Development Institute, Inc.
Posted 10/29/2015
NCT05060796RecruitingEarly Phase 1
Second Affiliated Hospital of Guangzhou Medical University
Posted 9/1/2019
NCT03182816Unknown StatusPhase 1
Shanghai Cell Therapy Research Institute
Posted 6/7/2017
NCT04348643Unknown StatusPhase 1
Chongqing Precision Biotech Co., Ltd
Posted 2/20/2020

Cancer Monoclonal Antibody Partnerships Surge with 599 Deals Recorded Since 2016

  • A comprehensive analysis reveals 599 cancer monoclonal antibody collaboration and licensing deals have been announced since 2016, demonstrating sustained industry investment in this therapeutic area.
  • The deals encompass multicomponent partnerships that typically begin with collaborative research and development and progress to commercialization of therapeutic outcomes.
  • Leading biopharma companies are actively pursuing cancer monoclonal antibody partnerships, with detailed financial terms including upfront payments, milestone payments, and royalty structures being tracked across transactions.
  • The report identifies the top 25 most active companies in cancer monoclonal antibody dealmaking, providing insights into partnership strategies and market dynamics in oncology therapeutics.

Bevacizumab Benefits in Colorectal Cancer Limited to Two-Year Window, New Analysis Reveals

  • A comprehensive review presented at the 2025 ASCO Gastrointestinal Cancers Symposium reveals bevacizumab (Avastin) provides survival benefits in colorectal cancer patients for approximately two years after initial administration.
  • Researchers found that after 20-24 months, the initial survival benefit from bevacizumab diminishes, potentially explaining the crossover of survival curves observed in the PARADIGM trial compared to panitumumab (Vectibix).
  • The study suggests bevacizumab treatment may lead to selection of more aggressive tumor clones over time, characterized by accelerated growth and invasiveness after the initial period of tumor stasis and shrinkage.

Defence Therapeutics Secures Key Patent Allowances for Accum® Multimer Technology and Vaccine Platform

  • Defence Therapeutics received USPTO Notice of Allowance for its Accum®-based multimer technology, covering molecular entities used in AccuTOX® and ARM® anti-cancer programs with patent protection extending to 2043.
  • The company secured US patent no. 12,150,989 for its vaccine platform technology, expanding protection for Accum®-based immunogenicity-enhancing variants derived from steroid acids.
  • Singapore Patent Office allowed Defence's counterpart vaccine technology application, with patent grant expected in early 2025, strengthening the company's global intellectual property portfolio.
  • These patent developments validate Defence's innovative approach and position the company for strategic partnerships and licensing agreements in the biotechnology sector.

CytomX Therapeutics Initiates Combination Therapy Arm in Phase 1 Melanoma Trial

  • CytomX Therapeutics has dosed the first patient in a combination arm studying CX-801 with Keytruda (pembrolizumab) for patients with metastatic melanoma.
  • The Phase 1 trial aims to evaluate safety, tolerability, and preliminary efficacy of this novel combination approach targeting advanced melanoma patients.
  • This study represents a significant step in exploring how CX-801's mechanism may potentially enhance the effectiveness of established immunotherapy treatments.

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