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TNGXNasdaq

Tango Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 2·Boston, MA, United States·CEO: Dr. Malte Peters M.D.
OncologyImmunologyPain

TNGX evidence brief

What we can confirm

BioSniper Score:
5.5 / 10
Market Cap:
$3.83B
Lead Asset:
TNG260 (Phase 1/Phase 2)

What it means

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

What to watch

Market Cap: $3.83B · Lead Asset: TNG260 (Phase 1/Phase 2)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · TNGX

Tango Therapeutics, Inc. (TNGX) is a clinical-stage biotechnology company developing precision cancer medicines, primarily focused on PRMT5 inhibitors for MTAP-deleted cancers, with no approved products and no revenue from product sales.

Key risk: No product revenue

5.5/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$3.83B

Cash Runway

—

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 8 clinical trials for Tango Therapeutics, Inc..

Similar companies

AI OverviewAI overview is shown in English only.

Tango Therapeutics, Inc. (TNGX) is a clinical-stage biotechnology company developing precision cancer medicines, primarily focused on PRMT5 inhibitors for MTAP-deleted cancers, with no approved products and no revenue from product sales.

  • Cash & equivalents of $345.6M as of 2026-06-30 [sec].
  • Total revenue of $0.0M and net income of -$55.3M as of 2026-06-30 [sec].
  • Lead PRMT5 inhibitor vopimetostat (TNG462) is in Phase 1/2 trials, with a pivotal study planned in second line pancreatic cancer in 2026 [sec · filed 2026-04-17].
  • TNG456, a brain-penetrant PRMT5 inhibitor, began Phase 1/2 dosing in May 2025 for CNS cancers including glioblastoma [sec_mda · as of 2026-08-11].
  • Cash runway extends into 2028, beyond anticipated key data inflection points [news · published 2026-05-13].

What works

  • Strong cash position of $345.6M as of 2026-06-30 provides runway into 2028 [sec].
  • Vopimetostat plus zoldonrasib combination showed a 52% ORR and 96% DCR in pancreatic cancer patients as of May 28, 2026 [sec_mda · as of 2026-08-11].
  • Multiple clinical programs advancing, including a planned pivotal study for vopimetostat in second line pancreatic cancer in 2026 [sec · filed 2026-04-17].

What to weigh

  • No approved products and no revenue from product sales; the company has never generated product revenue [sec_mda · as of 2026-03-05].
  • Net loss of $55.3M for the quarter ended 2026-06-30, with expenses expected to increase substantially [sec] [sec_mda · as of 2026-08-11].
  • Deprioritizing TNG260 program, indicating resource reallocation and potential pipeline narrowing [sec_mda · as of 2026-08-11].

From the filings

Quoted directly from source documents.

  • Vopimetostat plus zoldonrasib combination efficacy

    “We observed an ORR of 52%, a 16 74% six-month progression free survival rate, and 96% DCR in these patients.”

    SEC MD&A · August 11, 2026

  • No approved products and no product revenue

    “We have no products approved for commercial sale and therefore have never generated any revenue from product sales”

    SEC MD&A · March 5, 2026

  • Cash runway into 2028

    “Cash position of $380 million as of March 31, 2026, with runway into 2028 beyond anticipated key data inflection points”

    News · May 13, 2026

Catalyst timeline

  • 2022-03-23 · Phase2_Start: A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG908 in Patients With MTAP-deleted Advanced or Metastatic Solid Tumors — Initiation of Phase 1/2 trial for TNG908, an early PRMT5 inhibitor candidate.
  • 2023-05-26 · Phase2_Start: A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG462 as a Single Agent and in Combination in Patients With MTAP-deleted Advanced or Metastatic Solid Tumors — Start of Phase 1/2 trial for vopimetostat (TNG462), the lead PRMT5 inhibitor.
  • 2023-06-12 · Phase2_Start: A Phase 1/2, Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of TNG260 as a Single Agent and in Combination With an Anti-PD-1 Antibody In Patients With STK11 Mutated Advanced Solid Tumors — Initiation of Phase 1/2 trial for TNG260, which is now being deprioritized.
Risks & what to watch (3)›

Key risks

  • No product revenue — Company has never generated revenue from product sales and does not expect to in the foreseeable future [sec_mda · as of 2026-03-05].
  • Increasing expenses — Clinical development costs are expected to increase substantially with ongoing and planned trials [sec_mda · as of 2026-08-11].
  • Pipeline deprioritization — TNG260 program is being deprioritized and shut down, reducing pipeline diversity [sec_mda · as of 2026-08-11].

What to watch

  • Safety and efficacy update for vopimetostat monotherapy in lung cancer cohort expected in 2026 [sec_mda · as of 2026-08-11].
  • Initial clinical data from TNG456 Phase 1/2 trial anticipated in the second half of 2026 [sec_mda · as of 2026-08-11].
  • Phase 1/2 data from vopimetostat + RAS(ON) combination study in pancreatic cancer to be presented at 2026 ESMO Congress [news · published 2026-08-11].
  • Pivotal study initiation for vopimetostat in second line pancreatic cancer planned for 2026 [sec · filed 2026-04-17].

Sources: Catalysts · News · SEC filings · SEC MD&A · Generated October 12, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.9

D/E 0.05 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 1/Phase 2

Pipeline Breadth5.9

3 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal0.0

0 buys · 8 sells (180d)

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

194

Total value held

$3.73B

HolderSharesValue
rtw investments, lp13,300,620$278.2M
adage capital partners gp, l.l.c.12,809,485$268.0M
boxer capital management, llc10,876,219$227.5M
tcg crossover management, llc10,531,071$220.3M
fmr llc9,905,919$207.2M
farallon capital management llc9,097,411$190.3M
blackrock, inc.8,748,045$183.0M
woodline partners lp8,000,013$167.4M
nextech invest, ltd.7,266,081$152.0M
trv gp iv, llc6,374,574$133.4M

Showing top 10 of 194 institutional holders of Tango Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 22, 2026
% of float
26.9%
Days to cover
12.9
Shares short
38,250,843
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 →

TNGX short interest

Governance

Frequently asked questions

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

Tango Therapeutics, Inc. (TNGX) is a clinical-stage biotechnology company developing precision cancer medicines, primarily focused on PRMT5 inhibitors for MTAP-deleted cancers, with no approved products and no revenue from product sales.

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

Tango Therapeutics, Inc.'s most advanced tracked candidate is TNG260 (Phase 1/Phase 2) for Non Small Cell Lung Cancer.

Who is the CEO of Tango Therapeutics, Inc.?

Dr. Malte Peters M.D. is the chief executive officer of Tango Therapeutics, Inc. (TNGX).

Where is Tango Therapeutics, Inc. headquartered?

Tango Therapeutics, Inc. (TNGX) is headquartered in Boston, MA, United States.

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

Tango Therapeutics, Inc. develops therapies across Oncology, Immunology, Pain.

923 companies304,846 SEC filings22,720 clinical trials100% citation-verification pass rate (7d)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.