8-K ·Filed May 13, 2026

SPRO

Spero Therapeutics, Inc.
MIXED
Impact 5/10
Horizonweeks Processed4mo ago SEC0001193125-26-221567
8-K Item 2.02: Earnings release
Actionable Insight ◆ Mixed

The Q1 results are backward-looking and secondary to the June 18 FDA decision on tebipenem HBr. Monitor for any pre-PDUFA documents or commentary. Approval could trigger milestone payments and a re-rating; denial would likely require strategic alternatives given minimal revenue.

DirectionMixed
Confidencemedium
Horizonweeks
Final — all horizons settled through T+60d
SPRO ▼ -55.43% at T+60d
NEUTRAL call ✗ call lost -55.43% · α vs SPY -59.02% · entry $2.76 → $1.23
Entry anchored
May 13, 2026
via day open
T+1d
+1.09%
call +1.09% · α +2.31%
$2.79
settled 5mo ago
T+5d
-2.54%
call -2.54% · α -1.82%
$2.69
settled 5mo ago
T+20d
+3.26%
call +3.26% · α +4.12%
$2.85
settled 4mo ago
T+60d
-55.43%
call -55.43% · α -59.02%
$1.23
settled 8w ago

Price Chart

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Executive Summary

Spero Therapeutics reported Q1 2026 results with revenue plunging 95% to $0.3M as the Phase 3 trial ended, but net loss narrowed to $7.2M from $13.9M due to lower R&D expenses. Cash position grew to $56.1M, and guidance for runway into 2028 was reaffirmed. The market remains focused on the June 18 PDUFA decision for tebipenem HBr, which will determine the company's near-term trajectory.

Key Financial Metrics

EPS
$-0.13
Revenue
$258.0K
-95.6% YoY

Key Facts

  • Q1 2026 net loss of $7.2M vs $13.9M in Q1 2025 (narrowed 48%)
  • Diluted EPS: -$0.13 vs -$0.25 year over year
  • Total revenue fell to $0.3M from $5.9M, a 95% decline
  • R&D expenses dropped to $2.9M from $13.6M as PIVOT-PO trial completed
  • Cash and cash equivalents: $56.1M at March 31, 2026, up from $40.3M at year-end
  • Cash runway guidance maintained into 2028
  • PDUFA date for tebipenem HBr NDA remains June 18, 2026
  • GSK is the licensing partner for tebipenem HBr commercialization

Financial Impact

Revenue collapsed to near zero as collaboration milestones concluded; operating loss improved by ~$7M as clinical trial costs fell. No change to cash runway guidance.

revenuenet losscash

Risk Factors

  • FDA denial or complete response letter for tebipenem HBr
  • Revenue dependence on GSK milestones; no approved products
  • Dilution risk if additional financing needed post-PDUFA decision

Market Snapshot

Exchange
Nasdaq
Sector
Pharmaceutical Preparations
Analyst Consensus
0% bullish (6 analysts)

Investment Themes

Biotech & Drug Discovery

Documents Analyzed

This report is based on 6 SEC documents filed with EDGAR.

DocumentAccession Number
8-K Filing (Primary)0001193125-26-221567
Document: d147628d8k.htm0001193125-26-221567
Document: 0001193125-26-221567-index-headers.html0001193125-26-221567
Document: 0001193125-26-221567-index.html0001193125-26-221567
Document: 0001193125-26-221567.txt0001193125-26-221567
8-K Data (Synthetic)0001193125-26-221567
13 reports for SPRO
Performance horizon
63% Hit rate 5 of 8 directional calls best @ T+20▲ +14.59%Mar 26, 2026
Filters
Rows
Reports for SPRO — sortable, filterable
TypeNow
Sep 11, 2026
21d ago
EFFECT
BEARISH ★ 7/10
$1.13 $1.13· 0.00%▼ −0.34%$1.19 (−5.31%)
Aug 28, 2026
4w ago
8-K
BEARISH ★ 7/10
$1.22 $1.19▲ +2.46%▲ +2.32%$1.19 (+2.46%)
Aug 28, 2026
5w ago
S-3
BEARISH ★ 7/10
$1.22 $1.19▲ +2.46%▲ +2.32%$1.19 (+2.46%)
Aug 12, 2026
7w ago
Press Release
NEUTRAL ★ 4/10
$1.24 $1.22▼ −1.61%▲ +0.35%$1.19 (−4.03%)
Jul 14, 2026
11w ago
8-K
BULLISH ★ 8/10
$1.70 $1.44▼ −15.29%▼ −14.00%$1.19 (−30.00%)
Jul 14, 2026
11w ago
Press Release
BULLISH ★ 7/10
$1.70 $1.44▼ −15.29%▼ −14.00%$1.19 (−30.00%)
Jun 25, 2026
14w ago
8-K
NEUTRAL ★ 3/10
$2.26 $2.20▼ −2.65%▼ −4.82%$1.19 (−47.35%)
Jun 22, 2026
14w ago
8-K
BULLISH ★ 8/10
$2.15 $2.26▲ +5.12%▲ +4.10%$1.19 (−44.65%)
Jun 17, 2026
15w ago
Press Release
BULLISH ★ 8/10
$2.11 $2.10▼ −0.47%▲ +0.57%$1.19 (−43.60%)
May 13, 2026
20w ago
8-K
MIXED ★ 5/10
$2.76 $2.69▼ −2.54%▼ −1.82%$1.19 (−56.88%)
Showing 10 of 13

US Market Status

Market Closed — Opens Mon (64h 10m)

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