MAIA MAIA Biotechnology, Inc.

BULLISH Impact: 6/10 PRESS-RELEASE
Horizon months Filed Jun 3, 2026 Processed 9d 18h ago Wire GlobeNewswire
Press release: fda
Latest settled — T+1d
MAIA ▲ +4.90% at T+1d
LONG call ✓ call won +4.90% · α vs SPY +4.50% · entry $1.43 → $1.50
Next anchor: T+5d due 3d ago
Currently $1.30 · -9.09% from $1.43 entry
Entry anchored
Jun 3, 09:44 AM ET
via Databento tick
T+1d
+4.90%
call +4.90% · α +4.50%
$1.50
settled 9d ago
T+5d
call — · α —
due 3d ago
T+20d
call — · α —
in 19d
T+60d
call — · α —
in 3mo

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Executive Summary

MAIA Biotechnology announced FDA clearance of an IND amendment to open U.S. enrollment for the expansion of its Phase 2 THIO-101 trial of ateganosine in third-line NSCLC. This regulatory green light, combined with prior Fast Track designation, supports potential Accelerated Approval filing. The company plans up to five U.S. clinical sites, with initial site already active.

Actionable Insight

The IND clearance removes a key regulatory obstacle for U.S. trial expansion, de-risking the program for Accelerated Approval. Monitor enrollment updates and interim data from THIO-101 Parts C/D, as positive results could significantly impact valuation given the small market cap.

Key Facts

  • FDA cleared IND amendment allowing U.S. enrollment for Phase 2 THIO-101 expansion in third-line NSCLC.
  • First U.S. clinical site activated at Summit Medical Group in New Jersey; up to five sites planned in 2026.
  • Fast Track designation granted July 2025 enables rolling review and potential Accelerated Approval.
  • Phase 3 trial THIO-104 (pivotal) is actively screening patients for ateganosine plus CPI vs. chemotherapy.
  • Data from THIO-101 Parts A/B showed overall survival beyond two years for eight patients.

Financial Impact

No financial figures disclosed; pre-revenue clinical-stage company with $82M market cap.

Risk Factors

  • Phase 2/3 data may fail to meet endpoints, leading to clinical hold or approval denial.
  • Financing risk: company may need to raise capital to fund expanded U.S. trial and Phase 3.
  • Competition from approved NSCLC therapies (e.g., Keytruda, Opdivo) may limit commercial potential.

Market Snapshot

Exchange
NYSE
Sector
Pharmaceutical Preparations
Analyst Consensus
86% bullish (7 analysts)

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3306173
11 reports for MAIA
Performance horizon
100% Hit rate 5 of 5 directional calls best @ T+5▲ +14.52%Apr 8, 2026
Filters
Rows
Reports for MAIA — sortable, filterable
Type Now
Jun 3, 2026
9d ago
Press Release
BULLISH ★ 6/10
$1.43 $1.50▲ +4.90%▲ +4.50%$1.30 (−9.09%)
Jun 2, 2026
10d ago
Insider Cluster
BULLISH ★ 5/10
$1.35 $1.43▲ +5.93%▲ +6.62%$1.30 (−3.70%)
May 19, 2026
24d ago
DEFA14A
NEUTRAL ★ 2/10
$1.23 $1.29▲ +4.88%▲ +3.84%$1.30 (+5.69%)
May 14, 2026
29d ago
8-K
MIXED ★ 5/10
$1.26 $1.26· 0.00%▲ +0.06%$1.30 (+3.17%)
Apr 27, 2026
6w ago
DEFA14A
NEUTRAL ★ 2/10
$1.24 $1.25▲ +0.81%▲ +1.29%$1.30 (+4.84%)
Apr 16, 2026
8w ago
8-K
BULLISH ★ 7/10
$1.33 $1.35▲ +1.50%▲ +0.29%$1.30 (−2.26%)
Apr 8, 2026
9w ago
8-K
BULLISH ★ 7/10
$1.24 $1.20▼ −3.23%▼ −3.80%$1.30 (+4.84%)
Apr 7, 2026
9w ago
DEFA14A
NEUTRAL ★ 3/10
$1.20 $1.24▲ +3.33%▲ +0.79%$1.30 (+8.33%)
Mar 4, 2026
14w ago
Press Release
NEUTRAL ★ 5/10
$1.53 $1.54▲ +0.65%▲ +1.97%$1.30 (−15.03%)
Mar 3, 2026
14w ago
Press Release
BEARISH ★ 6/10
$1.51 $1.56▼ −3.31%▼ −2.55%$1.30 (+13.91%)
Showing 10 of 11

US Market Status

Market Closed — Opens Mon (53h 10m)

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