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IN8bio Presents Updated Overall Survival Data Surpassing 19.5 Months for DeltEx DRI in Newly Diagnosed Glioblastoma at ASCO 2026

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(High)
Rhea-AI Sentiment
(Positive)
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IN8bio (NASDAQ:INAB) reported updated data from its INB-200 Phase 1 and INB-400 Phase 2 studies of repeat-dose DeltEx DRI in newly diagnosed glioblastoma at ASCO 2026.

Median progression-free survival reached 13.0 months and median overall survival currently exceeds 19.5 months, versus 6.6 and 13.2 months for standard-of-care alone, with 43% vs 20% 24‑month survival and a generally well-tolerated safety profile.

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AI-generated analysis. Not financial advice.

Positive

  • mPFS 13.0 months vs 6.6 months with standard-of-care
  • mOS exceeds 19.5 months vs 13.2 months with standard-of-care
  • 24‑month survival 43% vs 20% for standard-of-care patients
  • No dose-limiting toxicities, CRS, or neurotoxicity reported
  • Cold-to-hot tumor microenvironment shift with broader T cell infiltration
  • Higher γδ T cell and CD4+ levels correlated with overall survival

Negative

  • Results based on 17 newly diagnosed glioblastoma patients treated
  • Median overall survival in repeat-dose cohort not yet reached
  • Data are early-phase from Phase 1 and Phase 2 studies

Key Figures

mPFS (repeat-dose DeltEx DRI): 13.0 months mPFS (SOC alone): 6.6 months mOS (repeat-dose DeltEx DRI): >19.5 months +5 more
8 metrics
mPFS (repeat-dose DeltEx DRI) 13.0 months Newly diagnosed GBM, up to six repeat doses
mPFS (SOC alone) 6.6 months Newly diagnosed GBM standard-of-care comparator
mOS (repeat-dose DeltEx DRI) >19.5 months Newly diagnosed GBM, not yet reached at data cutoff
mOS (SOC alone) 13.2 months Newly diagnosed GBM standard-of-care comparator
24‑month survival (DeltEx DRI) 43% Repeat-dose GBM patients alive at 24 months
24‑month survival (SOC) 20% SOC-only GBM patients alive at 24 months
Sample size 17 patients Newly diagnosed GBM treated with DeltEx DRI plus SOC
Historical SOC mOS ~14.6 months Stupp regimen GBM median overall survival since 2005

Market Reality Check

Price: $1.8700 Vol: Volume 92,940 is above th...
normal vol
$1.8700 Last Close
Volume Volume 92,940 is above the 20-day average of 66,210, indicating elevated interest into the ASCO update. normal
Technical Shares at $1.87 are trading just below the 200-day MA at $1.88, despite positive GBM survival data.

Peers on Argus

INAB gained 3.89% while momentum peers APRE and PCSA appeared in scanners with g...
2 Up

INAB gained 3.89% while momentum peers APRE and PCSA appeared in scanners with gains of about 7.37% and 7.42%. Scanner data flags this as stock‑specific rather than a broad sector rotation.

Common Catalyst Both INAB and peer APRE reported ASCO 2026 clinical data, pointing to conference-driven stock‑specific catalysts rather than a generalized biotech move.

Historical Context

5 past events · Latest: May 07 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
May 07 Q1 2026 earnings Positive -1.3% Reported GBM mPFS 13.0 vs 6.6 months SOC and cash of $21.9M.
May 06 Conference previews Positive -2.5% Announced upcoming γδ T cell data at ASCO and other 2026 meetings.
Apr 03 Inducement grants Neutral -2.1% Granted stock options for 11,800 shares to new employees.
Mar 12 FY 2025 earnings Positive -1.1% Highlighted durable GBM survival data and extended cash runway into H1 2027.
Feb 24 Conference appearance Neutral +2.6% Announced presentation and meetings at TD Cowen health care conference.
Pattern Detected

INAB has often traded lower after positive GBM and earnings updates, suggesting a pattern of selling into good news.

Recent Company History

Over the last few months, INAB has repeatedly highlighted DeltEx DRI GBM data with mPFS of 13.0 months vs. 6.6 months SOC and improving mOS, alongside strengthening its balance sheet via a private placement and reporting cash of $27.1M at year-end 2025 and $21.9M at Q1 2026. Despite clinically positive messages, shares often drifted lower after earnings and data‑focused releases. Today's ASCO update extends this GBM survival story with more mature mOS >19.5 months, fitting into an ongoing clinical narrative rather than a new program shift.

Regulatory & Risk Context

Active S-3 Shelf · $200,000,000
Shelf Active
Active S-3 Shelf Registration 2026-05-18
$200,000,000 registered capacity

An effective Form S-3/A shelf filed on May 18, 2026 permits IN8bio to offer up to $200,000,000 of various securities, enabling flexible capital raises via supplements like the $2,800,000 ATM registered on June 1, 2026.

Market Pulse Summary

This announcement highlights updated ASCO 2026 data for DeltEx DRI in newly diagnosed glioblastoma, ...
Analysis

This announcement highlights updated ASCO 2026 data for DeltEx DRI in newly diagnosed glioblastoma, with mPFS of 13.0 months and mOS exceeding 19.5 months versus SOC benchmarks of 6.6 and 13.2 months. The dataset remains small at 17 patients but shows encouraging survival and immunologic signals. Historically, INAB has repeatedly emphasized this GBM program and strengthened its financing tools, including a $200M shelf and a $2.8M ATM, making future clinical maturation and funding decisions key watchpoints.

Key Terms

median progression-free survival, median overall survival, gamma-delta (γδ) t cell, cytokine release syndrome, +3 more
7 terms
median progression-free survival medical
"Repeat dosing of DeltExTM Drug Resistant Immunotherapy (DRI) had a median progression-free survival (mPFS)..."
Median progression-free survival is the length of time at which half of patients in a clinical study have not experienced disease worsening or progression. Think of it like the moment in a race when 50% of runners have not yet crossed a trouble line—it shows how long a therapy can delay disease activity for a typical patient. Investors use it as a straightforward signal of a drug’s effectiveness that can influence regulatory approval, market demand, and revenue potential.
median overall survival medical
"and median overall survival (mOS) exceeding 19.5 months (not yet reached)."
Median overall survival is the middle point of how long patients live after starting treatment, meaning half live longer and half live shorter. It helps doctors understand how effective a treatment is and gives patients an idea of what to expect about their future.
gamma-delta (γδ) t cell medical
"developing innovative gamma-delta (γδ) T cell therapies and γδ T cell engagers..."
A gamma-delta (γδ) T cell is a small, specialized type of white blood cell that helps detect and attack infected or abnormal cells; unlike most T cells, it recognizes threats in a more general way and can respond rapidly. Investors pay attention because these cells are targets or tools in drug and cell‑therapy development, so data about their behavior can strongly influence a therapy’s effectiveness, safety profile, trial results, regulatory outlook and commercial potential — like a security team that shapes whether a new product is trusted and adopted.
cytokine release syndrome medical
"well tolerated, with no dose-limiting toxicities, cytokine release syndrome (CRS), or neurotoxicity..."
An intense immune overreaction in which the body's defense system releases a large surge of signaling proteins, causing fever, low blood pressure, breathing trouble or organ stress; imagine the immune system's alarm going into overdrive and flooding the body with emergency responders. Investors care because this side effect can slow or block regulatory approval, increase clinical trial costs and liabilities, limit how widely a therapy can be used, and therefore affect a drug's market value and sales potential.
tumor microenvironment medical
"drove a cold-to-hot tumor microenvironment shift, with broad T cell infiltration..."
The tumor microenvironment is the immediate area surrounding a cancer cell, made up of nearby cells, blood vessels, and support structures that influence how the cancer grows and spreads. It functions like a bustling neighborhood that can either help or hinder the tumor’s development. For investors, understanding changes in this environment can signal the effectiveness of treatments and potential shifts in a cancer-related market.
standard-of-care medical
"therapy in combination with the standard-of-care that has remained unchanged for over 20 years."
The standard-of-care is the widely accepted medical treatment or procedure that doctors typically use for a particular illness, based on current evidence and clinical practice. For investors it matters because new drugs or devices must beat or match this baseline to be adopted, reimbursed and widely sold—think of it as the default recipe a market expects; a new product must prove it’s tastier, cheaper, or faster to replace it.
phase 2 medical
"updated clinical data from its INB-200 Phase 1 and INB-400 Phase 2 studies..."
Phase 2 is the mid-stage clinical trial where a new drug or treatment is tested in a larger group of patients to see if it works and to keep checking safety after initial human testing. Think of it as a field test that proves whether a product actually delivers its promised benefit. Investors watch Phase 2 closely because its results strongly influence a medicine’s chances of reaching the market, the size of its potential sales, and the company’s valuation.

AI-generated analysis. Not financial advice.

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Repeat dosing of DeltExTM Drug Resistant Immunotherapy (DRI) had a median progression-free survival (mPFS) of 13.0 months and median overall survival (mOS) exceeding 19.5 months (not yet reached).

Results demonstrate the potential for meaningful improvement in outcomes with gamma-delta T cell therapy in combination with the standard-of-care that has remained unchanged for over 20 years.

NEW YORK, June 01, 2026 (GLOBE NEWSWIRE) -- IN8bio, Inc., a clinical-stage biopharmaceutical company developing innovative gamma-delta (γδ) T cell therapies and γδ T cell engagers (TCEs) for cancer and autoimmune diseases, today announced updated clinical data from its INB-200 Phase 1 and INB-400 Phase 2 studies at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting.

Among patients who received up to six repeat doses of genetically modified gamma delta (γδ) T cells (DeltEx DRI), median progression-free survival (mPFS) reached 13.0 months, nearly double the 6.6 months observed in patients receiving standard-of-care (SOC) alone. mOS has not yet been reached in repeat-dose patients and currently exceeds 19.5 months (+48%), compared to a final mOS of 13.2 months for patients receiving only SOC. Approximately 43% of repeat-dose patients remained alive at 24 months versus only 20% of SOC patients. Data are as of the May 15, 2026 data cutoff.

“These data continue to support the potential of DeltEx DRI to change the treatment landscape for newly diagnosed glioblastoma,” said William Ho, Chief Executive Officer and co-founder of IN8bio. “Patients today face the same outcomes as patients diagnosed over twenty years ago. Despite more than two decades with little advancement, we are seeing encouraging signals of durable disease control and prolonged survival supported by observed biomarker and immune reconstitution data. The need for new treatments for this devastating cancer is critical.”

Glioblastoma (GBM) is among the deadliest cancers. Despite the SOC combination of surgery, radiation, and temozolomide (TMZ) chemotherapy, known as the Stupp regimen, mOS has remained at only ~14.6 months since 2005. The data presented at ASCO included findings from 17 treated patients with newly diagnosed GBM receiving IN8bio’s DeltEx DRI γδ T cell therapy in combination with SOC, along with a comparison to contemporaneously enrolled patients receiving only the SOC.

The studies demonstrated that intracranially delivered DeltEx DRI was generally well tolerated, with no dose-limiting toxicities, cytokine release syndrome (CRS), or neurotoxicity events reported.

Additional translational analyses integrating histopathology with artificial intelligence (AI) technology demonstrated that DeltEx DRI treatment drove a cold-to-hot tumor microenvironment shift, with broad T cell infiltration and reduction in immunosuppressive granulocytes not observed in SOC patients. Repeat DeltEx DRI dosing resulting in higher total doses also increased cumulative γδ T cell and CD4+ levels that correlated significantly with overall survival, linking sustained immune reconstitution to improved outcomes in a dose-dependent manner. Taken together these data point to a γδ T cell-mediated local mechanism with systemic reach.

“These findings suggest DeltEx DRI may not only directly target residual tumor cells, but also help sustain immune competency during chemotherapy treatment,” said Kate Rochlin Ph.D., President and Chief Operating Officer of IN8bio. “The ability to preserve and restore key immune cell populations while driving local tumor microenvironment remodeling represents an important potential advancement in GBM immunotherapy.”

About INB-200 and INB-400

INB-200 and INB-400 are clinical-stage programs evaluating DeltEx DRI, IN8bio’s genetically modified gamma-delta T cell platform designed to resist the lymphodepleting effects of temozolomide chemotherapy. The therapy is intended to allow gamma-delta T cells to remain active during chemotherapy administration and target stress-induced ligands expressed on glioblastoma cells.

About IN8bio

IN8bio is a clinical-stage biopharmaceutical company developing γδ T cell and γδ T cell engager (TCE) product candidates to address unmet medical needs. γδ T cells are a specialized population of T cells that possess unique properties, including the ability to differentiate between healthy and diseased tissue. The Company’s pipeline is anchored by INB-600, a novel γδ T cell engager platform with potential applications across oncology and autoimmune indications. IN8bio is also advancing INB-100, an allogeneic γδ T cell candidate for adult patients with high-risk leukemias undergoing haploidentical stem cell transplantation, and INB-200/400, an autologous genetically modified γδ T cell candidate for newly diagnosed glioblastoma (GBM). For more information about IN8bio, visit www.IN8bio.com.

Investors & Company Contacts:

IN8bio, Inc.
Patrick McCall
646.933.5603
pfmccall@IN8bio.com

Media Contact
Kimberly Ha
KKH Advisors
917.291.5744
kimberly.ha@kkhadvisors.com


FAQ

What glioblastoma survival results did IN8bio (INAB) report for DeltEx DRI at ASCO 2026?

IN8bio reported median overall survival with repeat-dose DeltEx DRI currently exceeds 19.5 months. According to IN8bio, this compares with 13.2 months for patients receiving standard-of-care alone, with 43% of repeat-dose patients alive at 24 months versus 20% on standard-of-care.

How did DeltEx DRI affect progression-free survival in IN8bio's INB-200 and INB-400 studies?

DeltEx DRI achieved median progression-free survival of 13.0 months in newly diagnosed glioblastoma. According to IN8bio, this was nearly double the 6.6 months observed in contemporaneously enrolled patients who received only standard-of-care therapy, suggesting a clinically notable difference in time without disease progression.

What safety profile was observed with IN8bio's DeltEx DRI in newly diagnosed glioblastoma?

Intracranially delivered DeltEx DRI was described as generally well tolerated in the reported studies. According to IN8bio, no dose-limiting toxicities, cytokine release syndrome, or neurotoxicity events were observed among treated patients receiving the gamma-delta T cell therapy with standard-of-care.

How many patients were included in IN8bio's DeltEx DRI glioblastoma data presented at ASCO 2026?

The ASCO 2026 update included findings from 17 treated patients with newly diagnosed glioblastoma. According to IN8bio, these patients received DeltEx DRI gamma-delta T cells plus standard-of-care, with outcomes compared to contemporaneously enrolled patients who received only the standard Stupp regimen.

What immune and tumor microenvironment changes were linked to DeltEx DRI in INAB's glioblastoma trials?

DeltEx DRI treatment was associated with a cold-to-hot tumor microenvironment shift in glioblastoma. According to IN8bio, analyses showed broader T cell infiltration, reduced immunosuppressive granulocytes, and higher cumulative γδ T cell and CD4+ levels that significantly correlated with overall survival in a dose-dependent manner.

How does IN8bio's DeltEx DRI compare with the historical standard-of-care in glioblastoma?

DeltEx DRI plus standard-of-care showed median overall survival currently exceeding 19.5 months versus historical ~14.6 months since 2005. According to IN8bio, contemporaneous standard-of-care patients in these studies had 13.2-month median overall survival and 6.6-month median progression-free survival, highlighting differences versus the experimental regimen.

What is the mechanism IN8bio suggests for DeltEx DRI in improving glioblastoma outcomes?

IN8bio suggests DeltEx DRI may directly target residual tumor cells and support immune competency during chemotherapy. According to IN8bio, sustained γδ T cell and CD4+ reconstitution, plus tumor microenvironment remodeling, indicate a local γδ T cell–mediated mechanism with systemic reach in glioblastoma treatment.