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Pediatric remission case for Immatics (NASDAQ: IMTX) PRAME cell therapy

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6-K

Rhea-AI Filing Summary

Immatics N.V. reports that an abstract describing a pediatric case treated with its PRAME-directed TCR cell therapy has been accepted as a late-breaking poster at the AACR Annual Meeting 2026 in San Diego.

The case involves a 17-year-old with PRAME-positive advanced metastatic nephroblastoma who had exhausted standard treatment options. After receiving a TCR T-cell therapy using Immatics’ PRAME TCR encoded by the IMA203CD8 lentiviral vector, the patient achieved deep anti-tumor remission, first seen three months after infusion and ongoing at six months of follow-up. Imaging showed marked regression across lung, liver, brain and abdominal lesions, and liquid biopsy no longer detected tumor-derived DNA, indicating molecular remission. Cytokine release syndrome occurred but was described as manageable and resolved with multi-modal anti-cytokine therapy and corticosteroids. Immatics highlights PRAME as a target expressed in more than 50 cancers and plans to evaluate its PRAME TCR T-cell therapies in pediatric patients, including assessing a potential first-in-pediatrics Phase 1/2 basket study for relapsed or refractory PRAME-expressing solid tumors at KiTZ in Heidelberg.

Positive

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Negative

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AACR poster presentation date April 21, 2026, 2:00 pm PDT Timing of late-breaking clinical research poster on pediatric PRAME case
Patient age 17 years Adolescent with PRAME-positive advanced metastatic nephroblastoma
Abdominal lesion size 16 cm Longest diameter of abdominal tumor before treatment
Remission follow-up duration 6 months Deep remission ongoing six months after TCR T-cell infusion
Cancers expressing PRAME more than 50 cancers Extent of PRAME expression across tumor types
PRAME franchise components 3 product candidates, 2 modalities, 2 combinations Scope of Immatics’ PRAME-targeted pipeline
PRAME-directed TCR T-cell therapy medical
"Immatics is developing PRAME-directed TCR T-cell therapies engineered to recognize"
advanced metastatic nephroblastoma medical
"a 17-year-old adolescent with PRAME-positive advanced nephroblastoma, a malignant kidney cancer"
late-breaking poster presentation medical
"accepted for a late-breaking poster presentation at the American Association"
Phase 3 trial medical
"anzu-cel (anzutresgene autoleucel, IMA203) is currently being evaluated in a registration-enabling Phase 3 trial"
A Phase 3 trial is a large, late-stage test of a new drug or medical treatment done on many people to make sure it really works and is safe. For investors, it matters because a successful Phase 3 usually means the company can ask regulators to sell the product and could earn lots of money, while failure can sharply reduce the company’s value.
basket study medical
"including a potential first-in-pediatrics Phase 1/2 basket study in pediatric patients"
A basket study is a clinical trial that tests one treatment across several different diseases or tumor types that share a common biological feature, like the same genetic mutation. For investors, it matters because a single positive result can open the drug to multiple markets at once—think of a single key that might unlock many different doors—potentially speeding sales and stretching the commercial opportunity while concentrating development costs.
 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

 Washington, D.C. 20549

 

FORM 6-K

 

REPORT OF FOREIGN PRIVATE ISSUER PURSUANT TO RULE 13a-16 OR 15d-16 UNDER THE SECURITIES EXCHANGE ACT OF 1934

 

April 17, 2026


Commission File Number: 001-39363

 

IMMATICS N.V.

 

Paul-Ehrlich-Straße 15

72076 Tübingen, Federal Republic of Germany

(Address of principal executive office)

 

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F:

 

Form 20-F

  Form 40-F

 

 
 
 

INFORMATION CONTAINED IN THIS REPORT ON FORM 6-K

 

On April 17, 2026, Immatics N.V. (the “Company”) issued a press release announcing that an abstract highlighting a pediatric patient treated with a PRAME-directed cell therapy using the Company’s PRAME T-cell receptor (TCR) has been accepted for a late-breaking poster presentation at the American Association for Cancer Research (AACR) Annual Meeting 2026 in San Diego, California, USA.

 

EXHIBIT INDEX

 

Exhibit No. Description
99.1 Press release dated April 17, 2026

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

  IMMATICS N.V.
Date: April 17, 2026  
  By: /s/ Harpreet Singh
  Name: Harpreet Singh
  Title: Chief Executive Officer

  

 

 

 

 

 

 

Exhibit 99.1

 

 

 

 

PRESS RELEASE

 

PRAME-directed Cell Therapy Using Immatics’ TCR
Induces Deep and Durable Remission in Pediatric Patient
with Advanced Metastatic Nephroblastoma

 

·Individual experimental treatment attempt at Hopp Children’s Cancer Center Heidelberg (KiTZ) and Heidelberg University Hospital (UKHD) using a TCR T-cell therapy engineered with a PRAME-directed TCR provided by Immatics

 

·17-year-old adolescent with bulky, rapidly progressing nephroblastoma and no remaining treatment options achieved deep remission, including marked regression of liver, lung and brain metastases; response ongoing at 6 months of follow-up

 

·PRAME is a multi-pediatric cancer target, and findings highlight the therapeutic potential of PRAME TCR T-cell therapy in pediatric patients with solid tumors

 

·Data will be presented in a late-breaking poster at the AACR Annual Meeting 2026 by Dr. med. Christian M. Seitz, Group Leader at KiTZ

 

Houston, Texas and Tuebingen, Germany, April 17, 2026 Immatics N.V. (NASDAQ: IMTX, “Immatics” or the “Company”), the global leader in precision targeting of PRAME with multiple clinical-stage programs spanning cell therapies and bispecifics, today announced that an abstract highlighting a pediatric patient treated with a PRAME-directed cell therapy using Immatics’ PRAME T-cell receptor (TCR) has been accepted for a late-breaking poster presentation at the American Association for Cancer Research (AACR) Annual Meeting 2026 in San Diego, California, USA. The patient case will be presented on April 21, 2026, at 2:00 pm PDT (Late-Breaking Research: Clinical Research 3; Poster Section 52; Poster Board Number 7; Abstract Number LB326) by the treating physician, Dr. med. Christian M. Seitz, Group Leader at the Hopp Children’s Cancer Center Heidelberg (KiTZ).

 

The abstract highlights the case of a 17-year-old adolescent with PRAME-positive advanced nephroblastoma, a malignant kidney cancer that predominantly occurs in children. The patient had rapidly progressing disease with metastases to the lung, liver and brain with an abdominal lesion measuring 16 cm in longest diameter. After exhausting all available treatment options and being ineligible for any ongoing clinical trial, the treating physician requested Immatics’ PRAME-directed TCR (encoded by the IMA203CD8 lentiviral vector) for an individual experimental treatment attempt (named-patient use; “Individueller Heilversuch” in Germany) at KiTZ, where a TCR T-cell therapy was manufactured. Following treatment, the patient experienced a deep anti-tumor response, with remission observed three months post-infusion and ongoing at six months of follow-up. PET scan and MRI imaging demonstrated marked tumor regression across all lesion sites. Additionally, liquid biopsy monitoring showed no more tumor-derived DNA, indicating molecular remission. Safety events reported in the abstract by the treating physician included cytokine release syndrome, which was manageable and resolved under multi-modal anti-cytokine therapy and corticosteroids. At six months of follow-up, the patient is in excellent physical condition.

 

Immatics Press Release April 17, 20261| 4

 

“We are very grateful to Immatics for providing the PRAME-directed TCR that enabled us to reprogram the pediatric patient’s cells. We hope that possible further clinical evaluation may demonstrate the potential of PRAME-targeted cellular immunotherapies in helping other children and adolescents with cancer, as seen in this patient,” said Christian M. Seitz, M.D., treating physician and Group Leader of the Translational Immunotherapy group at KiTZ, German Cancer Research Center (DKFZ) and Heidelberg University Hospital (UKHD).

 

Cedrik Britten, M.D., Ph.D., Chief Medical Officer at Immatics, added, “Seeing such a profound response in a pediatric patient who had no treatment options left is both remarkable and deeply encouraging for everyone dedicated to making a meaningful impact on the lives of patients with cancer. It reinforces our belief in PRAME as a powerful target and highlights the potential of cell therapy for pediatric cancers, where tumors often show high PRAME expression. These results support continued evaluation of PRAME-directed cell therapies in pediatric cancers while exploring new therapeutic options for children facing such devastating diseases.”

 

PRAME is a tumor target present on the cell surface of more than 50 cancers and can be targeted by TCR T-cell therapies. Based on the high PRAME expression across multiple different pediatric tumors in combination with the potential benefit of particularly strong immune responses in young patients, PRAME TCR T-cell therapies may offer a promising new treatment option for these patients. Immatics is planning to evaluate the potential of its PRAME TCR T-cell therapy candidates in pediatric patients with cancer and is assessing multiple options for clinical development including a potential first-in-pediatrics Phase 1/2 basket study in pediatric patients with HLA-A*02:01-positive, PRAME-expressing relapsed or refractory solid tumors at KiTZ in Heidelberg.

 

About Immatics’ PRAME-Directed Cell Therapies

 

Immatics is developing PRAME-directed TCR T-cell therapies engineered to recognize an intracellular PRAME-derived peptide presented by HLA-A*02:01 on the surface of tumor cells and to initiate a potent and specific anti-tumor response.

 

Immatics’ PRAME-directed cell therapies are being evaluated in clinical trials across multiple PRAME-positive solid tumors in adult patients. Its lead PRAME cell therapy candidate, anzu-cel (anzutresgene autoleucel, IMA203) is currently being evaluated in a registration-enabling Phase 3 trial “SUPRAME” in previously treated advanced cutaneous melanoma and a Phase 2 trial in metastatic uveal melanoma. In addition, Immatics is evaluating its second-generation PRAME cell therapy, IMA203CD8, in a Phase 1a dose escalation trial in patients with PRAME-positive solid tumors, with a focus on gynecologic cancers.

 

About PRAME

 

PRAME is a target expressed in more than 50 cancers. Immatics is the global leader in precision targeting of PRAME and has the broadest PRAME franchise with the most PRAME indications and modalities. The Immatics PRAME franchise currently includes three product candidates, two therapeutic modalities and two combination therapies that target PRAME: anzu-cel (anzutresgene autoleucel, IMA203) PRAME cell therapy, IMA203CD8 PRAME cell therapy (GEN2), IMA402 PRAME bispecific as monotherapy and in combination with an immune checkpoint inhibitor as well as anzu-cel in combination with Moderna’s PRAME mRNA designed to enhance cell therapy.

 

Immatics Press Release April 17, 20262| 4

 

About Immatics

 

Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.

 

Immatics intends to use its website www.immatics.com as a means of disclosing material non-public information. For regular updates, you can also follow us on LinkedIn and Instagram.

 

Forward-Looking Statements

 

Certain statements in this press release may be considered forward-looking statements. Forward-looking statements generally relate to future events or the Company’s future financial or operating performance. For example, statements concerning timing of data read-outs for product candidates, observations from the Company’s clinical trials, the timing, outcome and design of clinical trials, the nature of clinical trials (including whether such clinical trials will be registration-enabling), the timing of IND, CTA or BLA filings, estimated market opportunities of product candidates, the Company’s focus on partnerships to advance its strategy, and other metrics are forward-looking statements. In some cases, you can identify forward-looking statements by terminology such as “may”, “should”, “expect”, “plan”, “target”, “intend”, “will”, “estimate”, “anticipate”, “believe”, “predict”, “potential” or “continue”, or the negatives of these terms or variations of them or similar terminology. Such forward-looking statements are subject to risks, uncertainties, and other factors which could cause actual results to differ materially from those expressed or implied by such forward-looking statements. These forward-looking statements are based upon estimates and assumptions that, while considered reasonable by Immatics and its management, are inherently uncertain. New risks and uncertainties may emerge from time to time, and it is not possible to predict all risks and uncertainties. Factors that may cause actual results to differ materially from current expectations include, but are not limited to, various factors beyond management's control including general economic conditions and other risks, uncertainties and factors set forth in the Company’s Annual Report on Form 20-F and other filings with the Securities and Exchange Commission (SEC). Nothing in this press release should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements, which speak only as of the date they are made. The Company undertakes no duty to update these forward-looking statements. All the scientific and clinical data presented within this press release are – by definition prior to completion of the clinical trial and a clinical study report – preliminary in nature and subject to further quality checks including customary source data verification.

 

Immatics Press Release April 17, 20263| 4

 

For more information, please contact:

 

  Media  
  Trophic Communications  
  Phone: +49 151 74416179  
  immatics@trophic.eu  

   

 

  Immatics N.V.  
  Jordan Silverstein  
  Head of Strategy  
  Phone: +1 346 319-3325  
  InvestorRelations@immatics.com    

  

 

Immatics Press Release April 17, 20264| 4

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FAQ

What did Immatics N.V. (IMTX) announce in this Form 6-K?

Immatics announced that an abstract on a pediatric patient treated with its PRAME-directed TCR cell therapy was accepted as a late-breaking poster at AACR 2026, highlighting a deep and durable remission in advanced metastatic nephroblastoma after all standard options were exhausted.

How did the pediatric patient described by Immatics (IMTX) respond to PRAME-directed therapy?

The 17-year-old with PRAME-positive advanced metastatic nephroblastoma achieved deep anti-tumor remission three months after infusion, which continued at six months. PET and MRI scans showed marked tumor regression across all lesions, while liquid biopsy detected no tumor-derived DNA, indicating molecular remission.

What safety events were reported for Immatics’ PRAME TCR treatment in this case?

The treating physician reported cytokine release syndrome as a safety event. It was described as manageable and resolved under multi-modal anti-cytokine therapy and corticosteroids, and at six months of follow-up the patient was reported to be in excellent physical condition.

How is Immatics (IMTX) planning to further develop PRAME-directed cell therapies in pediatrics?

Immatics plans to evaluate its PRAME TCR T-cell therapy candidates in pediatric cancers and is assessing options including a potential first-in-pediatrics Phase 1/2 basket study for HLA-A*02:01-positive, PRAME-expressing relapsed or refractory solid tumors at the Hopp Children’s Cancer Center Heidelberg (KiTZ).

What is PRAME and why is it important in Immatics’ oncology strategy?

PRAME is a tumor target expressed in more than 50 cancers and can be recognized by TCR T-cell therapies. Immatics positions itself as a global leader in precision PRAME targeting, with a franchise spanning multiple PRAME-directed cell therapies and bispecifics across various solid tumor indications.

Which PRAME-targeted product candidates are currently in Immatics’ pipeline?

Immatics’ PRAME franchise includes anzu-cel (anzutresgene autoleucel, IMA203) PRAME cell therapy, IMA203CD8 second-generation PRAME cell therapy, and IMA402 PRAME bispecific, as monotherapy and in combinations, including with an immune checkpoint inhibitor and Moderna’s PRAME mRNA to enhance cell therapy.

Filing Exhibits & Attachments

1 document