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TCRX

TScan Therapeutics, Inc.

Biological products·Phase 3·Waltham, MA, United States·CEO: Dr. Gavin MacBeath Ph.D.
Oncology

TCRX evidence brief

What we can confirm

BioSniper Score:
7.8 / 10
Market Cap:
$20.9M
Lead Asset:
tsc-100 (Phase 3)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $20.9M · Lead Asset: tsc-100 (Phase 3)
BioSniper AIPage context preserved

Prepared research question

What matters most for TCRX—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · TCRX

TScan Therapeutics (TCRX) is a clinical-stage biotechnology company developing TCR-engineered T cell (TCR-T) therapies for cancer, with a pipeline spanning hematologic malignancies and solid tumors, and is currently undergoing a strategic reorganization to focus on in vivo cell therapy for solid tumors.

Key risk: Capital insufficiency

7.8/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$20.9M

Cash Runway

—

Lead Asset

tsc-100 (Phase 3)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates for TScan Therapeutics, Inc..

AI OverviewAI overview is shown in English only.

TScan Therapeutics (TCRX) is a clinical-stage biotechnology company developing TCR-engineered T cell (TCR-T) therapies for cancer, with a pipeline spanning hematologic malignancies and solid tumors, and is currently undergoing a strategic reorganization to focus on in vivo cell therapy for solid tumors.

  • Cash and cash equivalents of $100.2M as of 2026-06-30 fund operations into the second quarter of 2027 [sec].
  • Total revenue of $1.1M and net loss of -$30.4M for the period ending 2026-06-30 [sec].
  • First patient dosed in Phase 3 ALLOHA-2™ study; topline readout expected mid-2028 [news · 2026-08-12].
  • Positive initial data from Cohort C of Phase 1 ALLOHA™ study reported, with 100% (13/13) patients showing complete donor chimerism [news · 2026-09-02].
  • Strategic reorganization announced in September 2026, including a ~75% workforce reduction and a pause in further enrollment in Phase 3 ALLOHA-2™ study due to insufficient capital [news · 2026-09-02].

What works

  • Positive initial data from Cohort C of Phase 1 ALLOHA™ study showed 100% (13/13) patients with complete donor chimerism, validating the commercial-ready manufacturing process [news · 2026-09-02].
  • Cash and cash equivalents of $100.2M as of 2026-06-30 provide a runway into Q2 2027, supporting ongoing operations [sec].
  • Two in vivo-engineered TCR-T candidates for solid tumors have advanced to IND-enabling studies, with plans to initiate Phase 1 development in Q4 2027 [news · 2026-09-02].

What to weigh

  • Net loss of -$30.4M for the period ending 2026-06-30, with total revenue of only $1.1M, indicating significant cash burn relative to revenue [sec].
  • Paused further enrollment in Phase 3 ALLOHA-2™ study of TSC-101 due to insufficient capital, and is actively seeking collaboration partners [news · 2026-09-02].
  • Workforce reduction of approximately 75% announced in September 2026, reflecting a major strategic downsizing [news · 2026-09-02].
  • Shareholders' equity of $69.0M against total debt of $32.5M as of 2026-06-30, indicating a leveraged balance sheet [sec].

From the filings

Quoted directly from source documents.

  • Cash runway into Q2 2027

    “Cash and cash equivalents fund operations into the second quarter of 2027”

    News · August 12, 2026

  • 100% complete donor chimerism in Cohort C

    “100% (13/13) patients currently being tracked show complete donor chimerism”

    News · September 2, 2026

  • Paused Phase 3 enrollment due to insufficient capital

    “Pauses further enrollment in Phase 3 ALLOHA-2™ study of TSC-101 due to insufficient capital”

    News · September 2, 2026

  • Workforce reduction of approximately 75%

    “Workforce reduction of approximately 75% and strategic”

    News · September 2, 2026

Catalyst timeline

  • 2022-11-01 · Phase1_Start: A Phase 1/3 Study Evaluating the Efficacy and Safety of T-Cell Receptor Engineered Donor T Cells in Subjects Undergoing Allogeneic Peripheral Blood Stem Cell Transplantation (ALLOHA-2) — Initiation of the Phase 1/3 ALLOHA-2 study; topline readout expected mid-2028.
  • 2024-05-06 · Phase1_Start: A Phase 1 Basket Study Evaluating the Safety and Feasibility of T-Plex, Autologous Customized T Cell Receptor-Engineered T Cells Targeting Multiple Peptide/HLA Antigens in Participants With Antigen-positive Locally Advanced (Unresectable) or Metastatic Solid Tumors — Initiation of the Phase 1 PLEXI-T solid tumor study.
  • 2026-06-18 · Phase3_Start: A Phase 1/3 Study Evaluating the Efficacy and Safety of T-Cell Receptor Engineered Donor T Cells in Subjects Undergoing Allogeneic Peripheral Blood Stem Cell Transplantation — Start of Phase 3 portion of the ALLOHA-2 study; enrollment later paused due to insufficient capital.
Risks & what to watch (4)›

Key risks

  • Capital insufficiency — Phase 3 ALLOHA-2™ study paused due to insufficient capital; seeking collaboration partners [news · 2026-09-02].
  • Workforce reduction — Approximately 75% workforce reduction announced in September 2026, impacting operational capacity [news · 2026-09-02].
  • Low revenue generation — Total revenue of $1.1M against net loss of -$30.4M as of 2026-06-30, indicating heavy reliance on funding [sec].
  • Competitive landscape — Pipeline candidates face numerous competitors in Phase 2/3 for hematologic malignancies [pipeline].

What to watch

  • Topline readout from Phase 3 ALLOHA-2™ study expected mid-2028 [news · 2026-08-12].
  • Initiation of Phase 1 development for in vivo-engineered TCR-T candidates for solid tumors planned in Q4 2027 [news · 2026-09-02].
  • Outcome of strategic collaboration partner search for ALLOHA-2™ study [news · 2026-09-02].
  • Cash runway into Q2 2027; monitor cash position and burn rate [sec].

Sources: Catalysts · News · Pipeline · Generated October 11, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health7.8

D/E 1.48 · 0% dilution

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth7.2

4 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Financials

Short Interest

as of Apr 28, 2026
% of float
2.4%
Days to cover
0.9
Shares short
942,877
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

TCRX short interest

Governance

Frequently asked questions

What is the AI investment thesis for TScan Therapeutics, Inc.?

TScan Therapeutics (TCRX) is a clinical-stage biotechnology company developing TCR-engineered T cell (TCR-T) therapies for cancer, with a pipeline spanning hematologic malignancies and solid tumors, and is currently undergoing a strategic reorganization to focus on in vivo cell therapy for solid tumors.

What is TScan Therapeutics, Inc.'s lead drug candidate?

TScan Therapeutics, Inc.'s most advanced tracked candidate is tsc-100 (Phase 3) for AML.

Who is the CEO of TScan Therapeutics, Inc.?

Dr. Gavin MacBeath Ph.D. is the chief executive officer of TScan Therapeutics, Inc. (TCRX).

Where is TScan Therapeutics, Inc. headquartered?

TScan Therapeutics, Inc. (TCRX) is headquartered in Waltham, MA, United States.

What therapeutic areas does TScan Therapeutics, Inc. focus on?

TScan Therapeutics, Inc. develops therapies across Oncology.

923 active companies304,861 SEC filings22,725 clinical trials
Citation log window (7 days): 13,363 recorded LLM calls; 0 block events, 0 warning events. These counts do not measure factual accuracy or research quality.Computed at
How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.