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Theravance Biopharma Inc

Theravance Biopharma Inc

TBPH
$16.93USD-0.24%-0.04 today

MARKET CAP

877.5M

P/E (TTM)

FWD P/E

8.7x

DAY RANGE

$17 – $17

52W RANGE

$11
$21

AI Summary

Stalk
Buy NowMedium

TBPH is exhibiting signs of structural repair with a Bullish Pivot Point pattern and price holding above key short-term EMAs. The intermediate trend is supported by mean-reversion dynamics, while the long-term uptrend remains intact. EMAs are flattening and turning higher, and RSI and Options Score show no exhaustion. The momentum-focused strategy favors participation on shallow pullbacks into rising EMA support.

  • $333M cash position and zero debt support trial funding
  • UPelry Q1 net sales $71.4M (+15% YoY); hospital doses +49%
  • Approval binary risk high: pending Phase III Cypress outcomes
Full analysis →

The case for & against

Bull & Bear analysis

Bullish

Theravance Biopharma, Inc. (NASDAQ: TBPH) is a biopharmaceutical company focused on developing innovative therapeutics for serious diseases, particularly in the field of rare neurological disorders and respiratory conditions. Its lead product, Amproloxetine, addresses neurogenic orthostatic hypotension (NOH) specifically associated with multiple system atrophy (MSA), while the commercial-stage product UPelry pertains to chronic obstructive pulmonary disease (COPD). With strategic pivots and strong financial backing, Theravance is positioning itself to capture significant market opportunities within the evolving biopharmaceutical landscape.

Bull says

  • $333M cash position and zero debt support trial funding
  • UPelry Q1 net sales $71.4M (+15% YoY); hospital doses +49%
  • Amproloxetine could become NOH standard of care if Phase III positive
  • Zymeworks deal adds R&D resources and reduces need for equity
  • 90% of neurologists would prescribe Amproloxetine upon approval
  • ~$175M in high-probability milestones expected over next 14 months

Bear says

  • Approval binary risk high: pending Phase III Cypress outcomes
  • Payers likely to demand step edits, slowing uptake
  • Long-term revenue uncertain beyond UPelry milestones
  • Elevated share volatility signals potential large swings
  • UPelry faces strong COPD competition from GSK and AZN
  • No dividend yield deters income-focused investors

Investment themes with TBPH

Pharmaceuticals -1.67%

Drug development driving global healthcare solutions

JNJ · LLY · RPRX
Demographics: Elderly Care -0.26%

Services and products for aging population

UCB.BR · JNJ · AZN

Earnings Call · Q1 2026 · Mgmt. Guidance

Updated 05-03-2026neutral

Transcript signals

Bull points

  • If ampryloxetine is FDA approved, it stands to be the first and only therapy to meaningfully improve symptoms of NOH and MSA beyond three to four weeks.
  • Current therapies provide inconsistent benefit, and only a third of MSA patients are actually receiving therapy. For the majority of patients treated, about half received mitodrine, a third received fludrocortisone, and about 10% received roxidopa, in addition to some off-label therapy use.
  • We see Amproloxetine as addressing an unmet need, not as competing in a crowded therapeutic space.

Bear points

  • I would anticipate that some payers, and I'm qualifying that, some payers may require step edits through current existing payments.
  • What we need to better understand and doing further work beyond that 40,000 is how many more patients out there perhaps are either undiagnosed or underdiagnosed.
  • I would anticipate that some payers, and I'm qualifying that, some payers may require step edits through current existing payments.
Read full transcript analysis ›