Register Now: From Clinical to Commercial: Accelerating ADC Late-Stage Development with Technology Innovation and Integrated Platform
News|Podcasts|March 4, 2026

The BioPharm Brief: New Glioblastoma Combo Immunotherapy Advances Adaptive Neuro-Oncology Trials

INOVIO and Akeso’s combination of DNA tumor antigen priming and dual checkpoint inhibition exemplifies adaptive trial strategies for challenging glioblastoma therapy.

Welcome to The BioPharm Brief, your daily snapshot of key developments in biopharmaceutical research and clinical innovation. Today we’re looking at a new collaborative immunotherapy approach for one of the most challenging solid tumors, glioblastoma multiforme, and what it could mean for future neuro‑oncology strategies.

INOVIO and Akeso have announced a clinical collaboration to evaluate a novel combination immunotherapy regimen for glioblastoma that involves integrating targeted DNA‑encoded tumor antigen priming with dual immune checkpoint inhibition. The partnership will investigate INO‑5412 (composed of INOVIO’s DNA immunotherapy candidates INO‑5401 and INO‑9012) in combination with Akeso’s bispecific antibody, cadonilimab, which targets both PD‑1 and CTLA‑4 pathways. This combination will be studied within the Phase II adaptive INSIGhT trial sponsored by Dana‑Farber Cancer Institute. Initial dosing is expected in the second half of 2026.

Glioblastoma remains a highly aggressive and often treatment‑refractory brain cancer, where median survival under current standard‑of‑care regimens has historically shown only modest improvement. The collaborative strategy aims to prime tumor‑specific immune responses while countering multiple immunosuppressive mechanisms within the tumor microenvironment. This approach has the potential to overcome the limitations seen with checkpoint inhibition alone. Previous exploratory studies combining INO‑5401 and immune checkpoint inhibitors have suggested meaningful immune activation, which has motivated the addition of dual checkpoint blockade in this next phase of investigation.

The use of an adaptive platform trial design like INSIGhT highlights a broader trend toward more efficient screening of experimental therapies in difficult‑to‑treat cancers by enabling multiple investigational arms to be assessed against a shared control. As immuno‑oncology continues to evolve, coordinated combination approaches that integrate antigen priming with enhanced checkpoint modulation may offer new avenues for addressing historically unmet needs in neuro‑oncology.

Thanks for listening to The BioPharm Brief. For analysis and expert insights, please visit BioPharmInternational.com.

Summary of key developments:

  • INOVIO and Akeso are collaborating on a combination immunotherapy regimen targeting glioblastoma’s complex immune resistance.
  • The INSIGhT adaptive trial will evaluate INO‑5412 plus cadonilimab beginning in late 2026.
  • Integrated strategies pairing immune priming with dual checkpoint blockade represent an emerging direction in solid tumor immunotherapy.


Related to this article

The BioPharm Brief: An AI-Designed Multibody ADC Enters the Clinic, Blackstone Backs Pfizer’s Monthly GLP-1, and enGene Readies a Bladder Cancer BLA
FDA clears the IND for Biolojic Design’s BD200, an AI-designed Trop2/Nectin-4 multibody ADC; Blackstone Life Sciences agrees to provide Pfizer up to $1.5 billion to develop its monthly GLP-1 receptor agonist berobenatide; and enGene Therapeutics plans a year-end BLA for detalimogene voraplasmid in BCG-unresponsive non-muscle invasive bladder cancer.
The BioPharm Brief: FDA Designations for a Bispecific CAR-T, a BLA for Friedreich’s Ataxia, and Phase 2b MASH Data for Efinopegdutide
FDA grants RMAT and Fast Track designations to AbelZeta’s CD20/CD19 bispecific CAR-T prizlon-cel in relapsed or refractory large B-cell lymphoma, Larimar Therapeutics completes a BLA seeking accelerated approval of nomlabofusp for Friedreich’s ataxia, and Merck’s GLP-1/glucagon receptor agonist efinopegdutide meets its primary endpoint in a phase 2b MASH trial.
The BioPharm Brief: argenx Bets on Peptides, a Two-Bispecific Regimen in Prostate Cancer, and a New Take on T-Cell Engagers
argenx agrees to acquire macrocyclic peptide developer Unnatural Products for up to about $1.15 billion, Johnson & Johnson’s pasritamig and JNJ-9401 bispecific regimen achieves a 73% PSA response in phase 1 in metastatic castration-resistant prostate cancer, and Janux Therapeutics’ TRBV6-targeted T-cell engager JANX011 shows deep B-cell depletion in healthy volunteers.
The BioPharm Brief: A Bispecific Approval in Head and Neck Cancer, TCR Bispecifics Head to the Clinic, and a New Antibody Target in Essential Thrombocythemia
FDA grants accelerated approval to Johnson & Johnson’s subcutaneous EGFR/MET bispecific Rybrevant Faspro for previously treated head and neck squamous cell carcinoma, T-Therapeutics raises a $133 million Series B to take TCR-CD3 bispecifics into clinical trials, and Alethio Therapeutics raises a $90 million Series A to advance its first-in-class G6B antibody for essential thrombocythemia.
The BioPharm Brief: Ivonescimab Priority Review in China, Stargardt Gene Therapy Moves Toward Phase 3, and Longer Dosing Intervals for an IBD Bispecific
China’s NMPA grants priority review to Akeso’s PD-1/VEGF bispecific ivonescimab with chemotherapy for first-line biliary tract cancer, VeonGen Therapeutics aligns with FDA on a phase 3 design for its dual-AAV Stargardt gene therapy VG801, and Caldera Therapeutics’ IL-23p19×TL1A bispecific CLD-423 shows a half-life of more than 40 days in a phase 1a trial.
The BioPharm Brief: A $7 Billion Oncology Option Deal, a TL1A Pivot, and Oral Adalimumab Heads to the Clinic
Boehringer Ingelheim licenses six preclinical ADC and T-cell engager programs from Sino Biopharmaceutical in a deal worth up to $7 billion, Spyre Therapeutics drops anti-TL1A antibody SPY072 in rheumatic diseases after phase 2 misses and turns to hidradenitis suppurativa, and Biora Therapeutics gets ethics approval for a first-in-human trial of its BioJet oral adalimumab capsule.