Terns Pharmaceuticals

TERNNASDAQHigh Risk

Small molecule drug development

Reviewed by Blane Jackson, DDS, MBA. Educational analysis only. Read the editorial policy and disclosures.

Market cap

Small cap

Cash position

$200M as of Q1 2025

~24 months runway (derived)

Revenue status

pre revenue

Pipeline assets

2 programs

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What does Terns Pharmaceuticals do?

Terns Pharmaceuticals is a small biotech company working on treatments for cancer, specifically a type of blood cancer called chronic myeloid leukemia (CML). Their main drug, TERN-701, is designed to block a protein that causes cancer cells to grow. Unlike older drugs, it attaches to a different part of the protein, which might help patients who have become resistant to current treatments. They also have a drug for an eye condition related to thyroid disease. For investors, Terns is a high-risk, high-reward bet: if their lead drug works well in clinical trials, it could become a major player in a multi-billion dollar market. But they face tough competition from an already-approved drug called asciminib, and they have no products on the market yet. The company has enough money to operate for about two years, but they'll need positive trial results to keep going. Keep an eye on their upcoming data releases, which could cause big stock price swings.

What to watch

1

Monitor for updated TERN-701 phase 1 data at major conferences like ASH or ASCO.

2

Track enrollment and dosing progress in the phase 1 trial via clinicaltrials.gov.

3

Watch for any announcements of partnerships or licensing deals for TERN-701.

4

Follow quarterly earnings calls for updates on cash runway and pipeline strategy.


Pipeline

DrugIndicationPhaseExpected data
TERN-701Chronic Myeloid Leukemia (CML)Phase 1Q4 2025
TERN-501Thyroid Eye Disease (TED)Phase 2H2 2026

Investment thesis

Bull case

Terns Pharmaceuticals is developing TERN-701, a potentially best-in-class allosteric inhibitor for CML, a well-established market with clear regulatory pathways. Early data suggest it may be more potent and safer than existing therapies, including asciminib. With a strong cash position and a second asset in TED, Terns offers multiple shots on goal. If TERN-701 demonstrates superiority in ongoing trials, it could capture significant market share and lead to a lucrative partnership or acquisition. The company's experienced management team and focus on precision medicine align with current oncology trends.

Bear case

Terns faces intense competition from Novartis's asciminib, which is already approved and has a head start. TERN-701 is still in early stages, and clinical data may not replicate preclinical promise. The CML market is relatively mature, and payers may be reluctant to switch patients without clear advantages. Additionally, Terns has no approved products and relies heavily on TERN-701's success; any clinical hold or safety issue could devastate the stock. The TED program is also competitive, with Amgen's Tepezza dominating. Terns may need to raise capital, diluting shareholders.

Key upcoming catalysts

Phase 1 data for TERN-701 in CML

Q4 2025

Unverified — this date has not been checked against a primary source.

Data ReadoutStock moving

Phase 2 interim data for TERN-501 in TED

H2 2026

Unverified — this date has not been checked against a primary source.

Data ReadoutSignificant

Presentation at ASH 2025

December 2025

Unverified — this date has not been checked against a primary source.

ConferenceModerate

Risk factors

Clinical trial failure or delay for TERN-701

Competitive pressure from asciminib and other CML therapies

Dependence on single lead asset for near-term value

Potential safety issues in early trials

Need for additional financing if trials expand

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Comparable companies

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Financial snapshot

These figures are drafted by our AI pipeline, not read from SEC filings. Confirm anything you would act on against the company's latest 10-Q or 10-K.

Cash

$200M as of Q1 2025

Q1 2025 — 6 quarters ago

Quarterly burn

$25M

Cash runway

~24 months

$200M ÷ $25M per quarter

Revenue

pre revenue

Institutional ownership

80%

Source: company profile text. These figures come from the company profile text, not from a filing we have parsed. Check them against the latest 10-Q before relying on them.

These figures are out of date

The cash position cited here is from Q1 2025, roughly 6 quarters ago. The company has almost certainly reported since. Check its latest filing before using any of this.

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Disclaimer: This page is for informational and educational purposes only and does not constitute financial advice or a recommendation to buy or sell securities. Clinical trial analysis reflects publicly available data and AI-generated interpretations. Biotech investing carries significant risk including potential total loss of investment. Always verify critical claims through primary sources and consult a qualified financial advisor. Some links on this page are affiliate links. Review our editorial policy and disclosures.

Cash against the next catalyst

Funded through this catalyst

Cash reaches roughly Q1 2027 on the disclosed figures, about 5 quarters past this Q4 2025 catalyst — the readout is funded without a raise.

  • Derived from $200M ÷ $25M per quarter, both self-reported.
  • Burn usually rises as a programme moves through late-stage trials, so this is an upper bound.
  • The cash figure is from Q1 2025, about 6 quarters ago. The company has almost certainly reported since.

This is the arithmetic between two dates, not a forecast. Companies raise early from strength, delay programmes, partner, or borrow.