Selected company directory

This public preview is selective and unranked. Use the member workspace for the complete research maps and comparisons.

Arvinas

On 2026-05-01, FDA approved vepdegestrant for certain ESR1-mutated ER+/HER2- advanced breast cancers. In August, the company reported completion of a global license to Rigel and expected future data from three Phase 1 programs.

Protein degradation / PROTAC

Syneron Bio

Both parties publicly confirmed the AstraZeneca collaboration. A 2026 financing announcement states that proceeds will advance the pipeline into clinical development; specific human oral PK data were not disclosed.

Oral cyclic peptides

Kymera Therapeutics

The 2026-10-29 announcement places KT-621 in Phase 2 for AD and asthma and reports Phase 1 healthy-volunteer results for KT-579. Sanofi is advancing KT-485 in Phase 1; Gilead is preparing a KT-200 CDK2 molecular glue IND.

Protein degradation / PROTAC

Oralead Pharma

The company website confirms the Macoral® / Simgut® platform and collaboration with BrightGene. The pipeline image reviewed is historical; current clinical stages require confirmation.

Oral cyclic peptides

Triastek

T25 is an oral octreotide acetate tablet. MED&SSE produces its shell and drug-containing core; FDA IND clearance was disclosed in 2026.

Oral cyclic peptides

Merck / MSD

LIPFENDRA is a U.S.-approved oral PCSK9 inhibitor. Its label confirms sodium caprate and approximately 1% oral bioavailability.

Oral cyclic peptides

Bachem

Provides process development, analytical services, and GMP clinical manufacturing for cyclic peptides, stapled peptides, and peptidomimetics. Classified as a manufacturing service provider; client drugs are not treated as proprietary pipelines.

Oral cyclic peptides

Nurix Therapeutics

The 2026-10-12 announcement reports the first participant enrolled in Phase 3 DAYBreak CLL-306. NX-5948 is an oral, brain-penetrant BTK degrader. The company also reported collaboration progress with Roche, Gilead, Pfizer, and Sanofi.

Protein degradation / PROTAC

Crystal NAX

Offers RNA synthesis, LNP / tLNP formulation screening, analytical characterization, and early-stage manufacturing. The website describes manufacturing as GMP-like for preclinical, toxicology, and IND-enabling programs; this should not be equated with full cGMP commercial manufacturing.

mRNA / LNP

Moderna

A publicly traded mRNA drug company with a disclosed platform spanning mRNA design, LNP delivery, and drug substance and drug product manufacturing.

mRNA / LNP

BioNTech SE

Develops cancer and infectious disease programs using immunotherapy and mRNA platforms; COMIRNATY is a named product with regulatory validation.

mRNA / LNP

Arcturus Therapeutics

Develops the LUNAR lipid delivery and STARR self-amplifying mRNA platforms. KOSTAIVE is an approved sa-mRNA COVID-19 vaccine.

mRNA / LNP

Acuitas Therapeutics

Founded in 2009, this LNP delivery technology company advances nucleic acid drug delivery R&D and commercialization primarily through partners. Licensed platforms are not classified as company-owned drug candidates.

mRNA / LNP

Candoo Pharmatech

This Canadian formulation provider uses QbD approaches for oral dosage form development and manufacturing process design, including immediate-release, controlled-release, bilayer, orally disintegrating, and sublingual products.

Formulation Development & Manufacturing

Catalent

Offers early development of small-molecule oral and injectable products. Its biologics business provides formulation, stability, and compatibility development for vials, prefilled syringes, and cartridges.

Formulation Development & Manufacturing

Veranova

Pharmorphix solid-state and particle engineering services are now part of Veranova, spanning screening, crystallization development, and analytical support.

Pharmaceutical solid state

Asymchem

Building on small-molecule CDMO, the company provides research and manufacturing for peptides, oligonucleotides, antibodies, conjugates, and drug products.

China-listed CRO/CDMO

Tigermed

Clinical CRO services include operations, regulatory affairs, pharmacovigilance, data management and statistics, SMO, and laboratories. Frontage is consolidated.

China-listed CRO/CDMO

Alnylam Pharmaceuticals

Alnylam develops RNA interference medicines and presents its delivery platforms, marketed products, clinical programs, and scientific materials on its official website. This profile identifies a drug developer, rather than a contract service provider.

Oligonucleotide Therapeutics & Delivery

Ionis Pharmaceuticals

Ionis describes a portfolio of RNA- and DNA-targeted medicines, with separate pipeline, medicines, clinical-trial, and scientific-publication resources. Product-specific mechanisms and development status should be checked against dated disclosures.

Oligonucleotide Therapeutics & Delivery

Wave Life Sciences

Wave develops RNA-targeting medicines using RNA interference and RNA editing approaches. Its October 27, 2026 update describes WVE-007 as an investigational GalNAc-siRNA and WVE-006 as an investigational RNA-editing oligonucleotide. These are distinct modalities, not mRNA products.

Oligonucleotide Therapeutics & Delivery

Dyne Therapeutics

Dyne describes its FORCE platform as a transferrin-receptor-binding Fab, linker, and therapeutic payload for muscle and CNS delivery. Oligonucleotide conjugation and candidate-specific clinical results should be assessed separately.

Oligonucleotide Therapeutics & Delivery

Certara

Certara offers model-informed drug-development services and biosimulation software. Its public portfolio includes Phoenix for PK/PD analysis and Simcyp for PBPK modeling, alongside development and regulatory support. Software availability does not establish a model's fitness for a particular decision.

Clinical Pharmacology & Model-Informed Development

Simulations Plus

Simulations Plus offers modeling and simulation software and consulting across discovery and development. Its public software portfolio includes GastroPlus, MonolixSuite, and QSP tools. Modeling choices and validation should follow the intended scientific question.

Clinical Pharmacology & Model-Informed Development

ICON plc

ICON lists population PK, PK/PD, exposure-response modeling, trial simulation, first-in-human dose prediction, and formulation-related IVIVC. These are service disclosures, not independent evidence of success for an individual project.

Clinical Pharmacology & Model-Informed Development

Aanastra

Aanastra discloses PEP-CAR, an anti-CD19 in vivo CAR-T strategy combining engineered RNA and targeting peptides for cancer and autoimmune disease. The public website does not establish a registered clinical program or validated patient outcomes.

In Vivo Cell Engineering & Gene Editing

AAVivo

AAVivo lists CD19 AVO-100, BCMA AVO-101, and dual BCMA/CD19 AVO-102 using T-cell-targeted AAV. The disclosed activities include vector production and construct optimization, not verified clinical dosing. AVO-103 is a TCR program and is kept separate from CAR-T.

In Vivo Cell Engineering & Gene Editing

Aera Therapeutics

AERA-109 is a targeted-LNP in vivo CAR-T candidate for B-cell-mediated autoimmune diseases, supported by mouse and nonhuman-primate studies. The pipeline projects clinical entry in the second half of 2026; a projected date is not proof that dosing has begun.

In Vivo Cell Engineering & Gene Editing

Alaya.bio

Alaya is a preclinical in vivo CAR-T developer. Its disclosed polymeric nanoparticle platform encapsulates lentiviral CAR vectors for targeted T-cell transduction; this is a hybrid polymer/viral approach, not simply a nonviral polymer delivery system.

In Vivo Cell Engineering & Gene Editing

AllerGene AI Therapeutics

AllerGene proposes in vivo-delivered mRNA CAR-T to target mast cells in allergic disease. Its website establishes research intent, but does not establish a named clinical candidate, patient dosing, or validated allergy outcomes. It is distinct from Allogene Therapeutics.

In Vivo Cell Engineering & Gene Editing

AlphaNa Bioscience

AlphaNa identifies AFN50 as an mRNA-based in vivo CAR-T program for autoimmune disease currently evaluated in IITs. The disclosed program is classified as investigator-initiated research; unrelated RNA programs and inconsistent codes elsewhere on the website are not used to infer additional CAR-T assets.

In Vivo Cell Engineering & Gene Editing

Intellia Therapeutics

Intellia presents CRISPR gene-editing science, clinical programs, and scientific publications on its official website. Its gene-editing work belongs in this broader in vivo engineering field; it should not be labeled as equivalent to in vivo CAR-T.

In Vivo Cell Engineering & Gene Editing

Beam Therapeutics

Beam develops investigational precision genetic medicines using base editing. Its website describes a delivery strategy spanning electroporation and nonviral and viral approaches. Those routes include different applications; the platform label alone does not establish in vivo efficacy.

In Vivo Cell Engineering & Gene Editing

Labcorp

Labcorp offers Bioanalytical testing and biomarker quantitation. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Resolian

Resolian offers Bioanalysis, DMPK and biomarker testing. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Parexel

Parexel describes clinical pharmacology, population PK, PK/PD, exposure-response, PBPK, dose justification, and noncompartmental analysis. Model assumptions, datasets, and intended regulatory use require project-specific review.

Clinical Pharmacology & Model-Informed Development

Tune Therapeutics

Tune develops TEMPO epigenetic regulation to activate or silence gene expression without cutting or changing the DNA sequence. Epigenetic modulation should be distinguished from sequence editing and permanent DNA insertion.

In Vivo Cell Engineering & Gene Editing

Sana Biotechnology

Sana develops CD8-targeted fusosome in vivo CAR-T, including SG293 and BCMA-directed SG227. Its August 2026 update describes SG293 clinical-start preparations and surrogate nonhuman-primate data, with SG227 clinical entry projected as early as 2027. Human dosing was not verified in this review.

In Vivo Cell Engineering & Gene Editing

Umoja Biopharma

VivoVec uses engineered lentiviral vectors for in vivo CAR-T. The disclosed pipeline includes CD22 UB-VV400/410 and BCMA×GPRC5D UB-VV500. IASO retains Greater China rights to the partnered CD22 programs; UB-VV111 is partnered with AbbVie. Trial registration and IND clearance do not establish efficacy.

In Vivo Cell Engineering & Gene Editing

EsoBiotec / AstraZeneca

AstraZeneca completed its acquisition in May 2025. ENaBL is a targeted lentiviral platform; anti-BCMA ESO-T01 has a published Phase 1 study in multiple myeloma. The small, uncontrolled study provides preliminary evidence, not established benefit.

In Vivo Cell Engineering & Gene Editing

Orna Therapeutics / Lilly

Orna develops circular RNA in vivo cell therapies, including CD19-directed ORN-252 for B-cell-driven autoimmune diseases. Lilly completed the acquisition in 2026; its Q3 filing identifies ORN-252 as Phase 1 at acquisition. ReNAgade was acquired by Orna in 2024 and is not counted separately.

In Vivo Cell Engineering & Gene Editing

Sail Biomedicines

Sail combines eRNA with targeted nanoparticles for in vivo CAR-T in immune-mediated diseases. Its July 2026 Johnson & Johnson collaboration includes an option to acquire Sail, not a completed acquisition. A named clinical CAR-T candidate is not established by this announcement.

In Vivo Cell Engineering & Gene Editing

Strand Therapeutics

The pipeline identifies STX-005 as a circular mRNA circuit for in vivo CAR-T in autoimmune disease and blood cancers. Clinical findings from the separate IL-12 programs STX-001/003 must not be attributed to STX-005; current CAR-T clinical initiation was not verified.

In Vivo Cell Engineering & Gene Editing

Azalea Therapeutics

Azalea develops enveloped delivery vehicles (EDVs) for targeted in vivo T-cell genome engineering. Its disclosed preclinical approach includes precise TRAC-locus CAR insertion. This combines delivery and site-specific integration; human therapeutic benefit has not been established.

In Vivo Cell Engineering & Gene Editing

Ensoma

Ensoma disclosed mouse proof of concept for in vivo HSC engineering that generates CAR-bearing macrophage, NK, and T-cell lineages. This is an HSC-derived, multi-lineage approach, distinct from directly transducing mature T cells. CAR-T human efficacy is not established.

In Vivo Cell Engineering & Gene Editing

NanoCell Therapeutics

NanoCell’s NanoCAR approach uses targeted LNPs to generate CAR-T cells in vivo. Its animal proof-of-concept disclosure describes nonviral DNA delivery; this should not be classified as a transient mRNA-only platform. Clinical efficacy remains unestablished.

In Vivo Cell Engineering & Gene Editing

Kernal Biologics

Kernal combines T-cell-targeted LNP delivery with selective mRNA translation for in vivo CAR-T. Its ASGCT 2026 announcement concerns preclinical programming studies. An ARPA-H award supports development; it is research funding, not clinical validation or a venture financing round.

In Vivo Cell Engineering & Gene Editing

EXUMA Biotech

EXUMA’s GCAR platform combines CD3-targeted lentiviral delivery with FITNESS DRIVER for in vivo CAR engineering. Its separate rPOC SC platform incubates PBMCs with vector outside the body and should not be described as fully in vivo manufacturing. Current GCAR clinical stage was not verified.

In Vivo Cell Engineering & Gene Editing

Tempest Therapeutics

TPST-4003 combines CD7-targeted mRNA/LNP delivery with a CD19/BCMA CAR; first IIT dosing was projected for Q4 2026, not verified as completed. Tempest separately obtained an option to license Senlang’s clinical lentiviral platform. TPST-2003 clinical results concern ex vivo CAR-T.

In Vivo Cell Engineering & Gene Editing

Hebei Senlang Biotechnology

Senlang’s CD7-targeted lentiviral in vivo CAR-T portfolio includes a BCMA/GPRC5D candidate in Phase 1 dose escalation for relapsed/refractory myeloma. Partner Tempest disclosed an exclusive option in September 2026; an option is not an exercised license or acquisition.

In Vivo Cell Engineering & Gene Editing

CREATE Medicines

CREATE, formerly Myeloid Therapeutics, disclosed preclinical in vivo CAR-T/CAR-NK and all-RNA RetroT work at AACR 2026. Clinical MT-302 is a myeloid-cell program, not evidence that its CAR-T programs have reached the same stage. The former name is retained as an alias.

In Vivo Cell Engineering & Gene Editing

Vyriad

Vyriad develops targeted viral genetic medicines and oncolytic therapies. Its BCMA-directed in vivo CAR-T candidate VV169 uses a retargeted lentiviral vector to engineer T cells inside the body. On September 10, 2026, the company announced that its Phase 1 study in relapsed/refractory multiple myeloma was open for enrollment at Mayo Clinic following FDA IND clearance. Patient dosing and clinical benefit were not established in that announcement.

In Vivo Cell Engineering & Gene Editing

CPTx

CPTx develops single-stranded DNA payloads with nonviral LNP delivery for in vivo CAR-T. The company reports small-animal validation; durability, redosing, and immune-silence statements remain company claims. CPTx is a distinct company from Capstan and the CPTX2309 drug code.

In Vivo Cell Engineering & Gene Editing

Legend Biotech

LB2501 is a CD19/CD20 in vivo CAR-T candidate using the TaVec lentiviral platform, with an ongoing China Phase 1 study (NCT07002112). Its October 2026 U.S. IND clearance supports a planned Phase 1/2 study. Neither IND clearance nor early responses constitute approval.

In Vivo Cell Engineering & Gene Editing

IASO Biotherapeutics

IASO reported first-in-human Phase 1 data for BCMA-directed IASO206 in relapsed/refractory myeloma at IMS 2026. It also partners with Umoja on CD22 programs with territorial rights. IASO206 and Umoja’s CD22 UB-VV400 are different programs.

In Vivo Cell Engineering & Gene Editing

Immorna

Immorna reports clinical investigation of JCXH-213, an RNA-based in vivo CAR-T candidate, in autoimmune diseases including ITP and systemic sclerosis. These are company-reported early findings, not proof of comparative efficacy; separate vaccine stages do not establish this program’s stage.

In Vivo Cell Engineering & Gene Editing

GRIT Biotechnology

GRIT disclosed T-cell-targeted mRNA/LNP GT801 and a separate lentiviral direction. GT801 is also developed through spinout Vivacta Bio; the two company profiles describe a shared program lineage, not two independent drugs. GRIT’s TIL clinical stages are separate.

In Vivo Cell Engineering & Gene Editing

Genocury Biotech

Genocury’s September 2025 announcement reports an investigator-initiated study of CD19-directed in vivo CAR-T in B-cell lymphoma. A reported individual response is preliminary and does not establish durability or comparative benefit. Current enrollment and formal regulatory trial status need confirmation.

In Vivo Cell Engineering & Gene Editing

MagicRNA Biotechnology

HN2301 delivers CD19 CAR mRNA using engineered T-cell-targeted LNPs. MagicRNA reports first-in-human SLE findings published in the New England Journal of Medicine. The older English homepage’s IND-enabling description is not used to override the later human-study disclosure.

In Vivo Cell Engineering & Gene Editing

Starna Therapeutics

Starna’s pipeline includes STR-P004 and STR-P005 in vivo CAR-T programs for autoimmune disease. An ASCO abstract describes CD19 CAR mRNA in CD8-targeted LNPs and exploratory patient dosing for STR-P004. These early findings do not establish efficacy or the stage of STR-P005.

In Vivo Cell Engineering & Gene Editing

Simnova Biotherapeutics

Simnova holds Greater China development and commercialization rights for partnered Orna in vivo cell therapies. The January 2025 expansion adds BCMA to the circular RNA partnership. Territorial participation is retained without counting the partnered programs as unrelated inventions; current clinical stage was not verified.

In Vivo Cell Engineering & Gene Editing

Immunofoco

Immunofoco’s iMagic platform uses a fusogen and T-cell-targeting modules for in vivo CAR-T. It identifies CD19 IMV101 in IITs, alongside BCMA IMV102 and CLDN18.2 IMV103. Phase 3 IMC002 is an ex vivo program and does not establish in vivo Phase 3 development.

In Vivo Cell Engineering & Gene Editing

Oricell Therapeutics

Oricell explicitly lists OriV508, a CD19/BCMA in vivo CAR-T program, as IIT ongoing, and OriV118 targeting GPRC5D/BCMA. The pipeline does not establish the delivery platform or OriV118’s current stage. Its ex vivo OriCAR-017 data must be kept separate.

In Vivo Cell Engineering & Gene Editing

Vivacta Bio

Vivacta is a GRIT in vivo CAR-T platform spinout developing CD19 mRNA/tLNP candidate GT801. A first-in-human study is registered as NCT07205315. Its October 2026 U.S. orphan designation for AIHA is not approval or proof of efficacy; GT801 is shared with the GRIT profile.

In Vivo Cell Engineering & Gene Editing

Byterna Therapeutics

BR101 is a BCMA/CD19 circular mRNA in vivo CAR-T program in a registered IIT for relapsed/refractory myeloma (NCT07537049). Autoimmune development and BR102/BR103 are separately described as preclinical; their stages should not be inferred from BR101.

In Vivo Cell Engineering & Gene Editing

RiboX Therapeutics

RXIM002 uses targeted LNPs carrying CD19 CAR circular RNA. The August 2026 update reports ongoing China IIT follow-up and FDA IND clearance for autoimmune cytopenias. It also discloses a fatal serious adverse event in a participant with systemic sclerosis; causality should not be inferred.

In Vivo Cell Engineering & Gene Editing

Stylus Medicine

Stylus combines engineered recombinases with cell-targeted LNP delivery to create durable in vivo CAR-T through sequence-specific insertion. Its platform disclosure establishes preclinical research intent and mechanism, not patient benefit or demonstrated clinical safety.

In Vivo Cell Engineering & Gene Editing

GenVivo

GenVivo identifies GEN-310 as an in vivo CAR-T/NK program for B-cell malignancies. Its October 2025 corporate presentation classifies GEN-310 as preclinical. Clinical work on separate immunocytokine vectors should not be used to upgrade this CAR program.

In Vivo Cell Engineering & Gene Editing

Cellinfinity BIO

Manufacturing partner uBriGene identifies Cellinfinity’s CIB-301 and CIB-350 as in vivo CAR-T programs for hematologic and solid tumors, supported by lentiviral vector manufacturing. The March 2026 announcement does not establish a registered clinical phase or human efficacy.

In Vivo Cell Engineering & Gene Editing

Jenthera Therapeutics

Jenthera discloses an in vivo autologous CAR-T reprogramming program in B-cell lymphoma using targeted ribonucleoprotein genome editing and homology-directed insertion. Website tumor-eradication statements do not establish human efficacy.

In Vivo Cell Engineering & Gene Editing

ModeX Therapeutics / OPKO

ModeX, an OPKO company, lists MDX3001 as in vivo CAR-T for cancer and autoimmunity. Its platform conjugates CD3×CD28 antibodies to LNPs carrying CAR mRNA. Human dosing and the program’s precise current stage were not established by the accessible pipeline text.

In Vivo Cell Engineering & Gene Editing

Thesian Bio

Thesian’s ARIANE platform uses in vivo engineering to generate CAR-T and CAR-macrophages for oncology and autoimmune disease. The company describes lentiviral engineering expertise and a dual-lineage approach. A named clinical-stage candidate and patient efficacy were not verified.

In Vivo Cell Engineering & Gene Editing

GigaMune

GigaMune develops diverse viral pseudotypes for repeat-dose in vivo CAR-T delivery and shows anti-CD19 mouse proof of concept. Proposed sequential dosing and immune evasion are platform hypotheses; human redosing safety and efficacy have not been established.

In Vivo Cell Engineering & Gene Editing

YolTech Therapeutics

YolTech explicitly lists YOLT-401 for autoimmune disease as an in vivo CAR-T program with an undisclosed target. Its clinical gene-editing programs are separate; their stages and delivery details are not automatically assigned to YOLT-401.

In Vivo Cell Engineering & Gene Editing

Immugenia

Immugenia discloses lentiviral in vivo CAR delivery to T/NK cells and HSCs, with promoter-restricted expression in T/NK lineages. HSC-derived replenishment differs from direct mature-T-cell engineering. The public disclosure does not establish a current CAR-T clinical phase.

In Vivo Cell Engineering & Gene Editing

Hemogenyx Pharmaceuticals

An October 2026 company announcement describes an in vitro feasibility study combining FLT3 CAR mRNA with Nitto’s cell-targeted LNPs. This is an early in vivo CAR-T development effort, not human in vivo treatment. Clinical HG-CT-1 is a separate ex vivo product.

In Vivo Cell Engineering & Gene Editing

Nona Biosciences

Nona supplies antibody discovery and CAR screening for Umoja’s in vivo CAR-T collaboration. The November 2025 agreement assigns subsequent product development and commercialization to Umoja. Nona is labeled an enabling partner, not a separately confirmed clinical CAR-T developer.

In Vivo Cell Engineering & Gene Editing

uBriGene Biosciences

uBriGene provides lentiviral process development, GMP manufacturing, and regulatory support for Cellinfinity’s in vivo CAR-T programs. Its manufacturing partnership establishes an enabling role; it does not establish ownership of the therapeutic candidates.

In Vivo Cell Engineering & Gene Editing

Axelyf

Axelyf identifies AX-004 as its proprietary in vivo CAR-T candidate for solid tumors using AXL LNP delivery. Disclosed support is from mouse and non-human-primate studies; human dosing or clinical efficacy is not inferred.

In Vivo Cell Engineering & Gene Editing

Mote Therapeutics

Founded in 2023 and headquartered in Lexington, Mote was created by Fapon Group and Alex Wesselhoeft. Its mobilize platform enables targeted LNP/circRNA delivery. Its BIO 2026 presentation identifies a preclinical CD19/BCMA in vivo CAR-T lead; a projected November IIT is not proof of dosing.

In Vivo Cell Engineering & Gene Editing

Mana.bio

Mana.bio applies machine learning to LNP design and disclosed a 2026 ASGCT presentation on progress toward in vivo CAR-T. The accessible material supports delivery-platform research; a named therapeutic candidate, clinical initiation, and patient efficacy were not verified.

In Vivo Cell Engineering & Gene Editing

Pregene Biopharma

The ESO-T01 Phase 1 publication includes a Pregene-affiliated coauthor alongside EsoBiotec. This establishes participation in the published work, not independent ownership of ESO-T01 or a separate verified in vivo CAR-T pipeline. Commercial rights require further confirmation.

In Vivo Cell Engineering & Gene Editing

Velvet Therapeutics

Velvet discloses amino-acid nanoparticles and minicircle DNA for in vivo CAR delivery to multiple immune-cell types. The accessible primary page does not specify a T-cell program or clinical stage; it is retained as an adjacent CAR platform rather than counted as a confirmed CAR-T developer.

In Vivo Cell Engineering & Gene Editing

Singular Immune

Singular’s iCAR is a recombinant fusion-protein approach to modifying T or NK cells in vivo. It is kept separate from gene-encoded CAR-T because protein-based receptor installation has a different mechanism. The website does not establish human efficacy.

In Vivo Cell Engineering & Gene Editing

ImmunoVec

ImmunoVec develops programmable DNA with cell-type-specific transcriptional control; the accessible primary disclosure highlights NK cells. It is tracked as adjacent in vivo immune engineering, without assuming that CAR-NK results establish a CAR-T program or clinical stage.

In Vivo Cell Engineering & Gene Editing

Liberate Bio

Liberate’s RAPTOR delivery platform supports initial in vivo CAR-macrophage programs through monocyte/macrophage reprogramming. CAR-M is a neighboring modality, not CAR-T; these programs are not included in the confirmed CAR-T developer count.

In Vivo Cell Engineering & Gene Editing

ImmTune Therapies

ImmTune discloses delivery vectors for in-body cell and gene therapy. Its accessible updates are old and do not establish a current named CAR-T program or clinical status. It remains a platform watchlist entry, outside the confirmed CAR-T developer count.

In Vivo Cell Engineering & Gene Editing

Tidal Therapeutics / Sanofi

Sanofi acquired Tidal in April 2021 for its nanoparticle mRNA platform for in vivo immune-cell reprogramming, including CAR-T applications. This is a historical acquired-platform record; the original preclinical description is not a verified current program stage or an independent active biotech.

In Vivo Cell Engineering & Gene Editing

RSSL

Reading Scientific Services (RSSL) offers Biologics structure, glycans, impurities, GMP release and stability. Services should be matched to the intended study and assay requirements.

Biologics Characterization & CMC Analytics

Sannova Analytical

Sannova Analytical offers Bioanalytical development and preclinical/clinical sample analysis. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

CellCarta

CellCarta offers Flow cytometry, histopathology, genomics and protein biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Anapharm

Anapharm offers Small- and large-molecule bioanalysis, PK and immunogenicity. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

KCAS Bio

KCAS Bio offers PK, immunogenicity, flow cytometry and biomarker testing. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

QPS

QPS offers Small- and large-molecule bioanalysis, immunogenicity and biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Celerion

Celerion offers Clinical PK, mass spectrometry, immunoassays and biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Cerba Research

Cerba Research offers PK, immunogenicity, flow cytometry and clinical biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Inotiv

Inotiv offers DMPK, clinical bioanalysis and biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

PharmaLegacy

PharmaLegacy offers Preclinical biomarkers, flow cytometry and immunoassays. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

InnoStar

益诺思 (InnoStar) offers PK/TK, clinical bioanalysis and translational biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

JOINN Laboratories

昭衍新药 (JOINN Laboratories) offers PK, immunogenicity, molecular assays and bioanalysis. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Sun-Novo

阳光诺和 (Sun-Novo) offers Clinical bioanalysis and bioequivalence services. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

ADICON

艾迪康 (ADICON) offers Clinical-trial central laboratory, molecular pathology and biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

KingMed

金域医学 (KingMed) offers Clinical-trial central laboratory and biomarker testing. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

SCL Healthcare

SCL Healthcare offers Clinical-trial laboratory, mass-spectrometry PK and biomarker development. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

BioInfra

BioInfra offers Bioanalytical sample testing and bioequivalence studies. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Biotoxtech

Biotoxtech offers Preclinical bioanalysis and PK/TK, including Keyfron Bio services. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

HLB bioStep

HLB bioStep offers Preclinical PK/TK, mass spectrometry, flow cytometry and biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Novotech

Novotech offers Large-molecule PK, ADA, neutralizing antibodies and clinical laboratory testing. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Lablytica

Lablytica offers Regulated small- and large-molecule bioanalysis and biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Admescope

Admescope offers Non-GLP quantitative bioanalysis, DMPK and biomarker studies. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Chimera Biotec

Chimera Biotec offers Ultrasensitive immunoassays, large-molecule bioanalysis and biomarkers. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Biognosys

Biognosys offers Mass-spectrometry proteomics, metabolomics and biomarker research. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Metabolon

Metabolon offers Metabolomics and biomarker discovery and analysis. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Allumiqs

Allumiqs offers Mass-spectrometry proteomics, multiomics and biomarker discovery. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

Syneos Health

Syneos Health offers Small- and large-molecule PK, immunogenicity and biomarker testing. Services should be matched to the intended study and assay requirements.

Bioanalysis & Biomarkers

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