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INDV drug pipeline

Supernus, Inc. · 2 rated drugs
Next catalyst
None dated
No dated FDA catalyst on file
Typical move on FDA news
±5.1%
1-day, median of 3 events
IV rank
16
IV 44% · HV 30%
Rated drugs
2
2 bearish
Phase 3 trials
0
0 with results posted

Drugs

soonest catalyst first
▼ bearish
Impact
PhaseApproved
Time to marketAlready approved. However, Indivior discontinued all marketing and promotion of OPVEE in September 2025 after a settlement with the New York Attorney General over misleading sales tactics. The drug is effectively off the commercial market.

OPVEE nalmefene hydrochloride Updated Oct 29

What to watch

OPVEE by itself has no catalysts left to watch. For INDV stock, the near-term events are the Supernus merger closing (expected November 2, 2026), after which the combined company will trade under ticker SUPN. The merger makes OPVEE's commercial failure even less relevant, as the combined entity will have a diversified CNS pipeline beyond opioid-use-disorder products.

Bull case
  • OPVEE was the first FDA-approved nalmefene nasal spray for opioid overdose, differentiated from naloxone by a longer duration of action that could theoretically be advantageous against potent synthetic opioids like fentanyl.
  • The FDA approval was a scientific/regulatory validation of nalmefene as an alternative to naloxone for overdose rescue.
Bear case
  • Indivior discontinued all marketing and promotion of OPVEE in September 2025, following a settlement with the New York Attorney General over allegations it misled public officials about the drug's authorization and effectiveness.
  • OPVEE was a commercial failure: it generated meager sales and was never adopted by health departments or harm-reduction organizations who preferred naloxone (Narcan), which is available over-the-counter and has a better safety profile.
  • Harm reduction advocates actively opposed OPVEE, arguing it caused more severe withdrawal symptoms than naloxone and offered no meaningful advantage at a higher price.
▼ bearish
Impact
PhaseApproved / Discontinued
Time to marketPERSERIS was already FDA-approved (July 2018) and marketed until its discontinuation. It is no longer available for prescription as of May 31, 2026.

PERSERIS risperidone Updated Oct 29

What to watch

PERSERIS is a fully discontinued product with zero revenue contribution and no remaining catalysts. The stock's value story now rests entirely on SUBLOCADE's commercial trajectory and the pending Supernus merger (expected Q4 2026); PERSERIS is irrelevant to future price action.

Bull case
  • The discontinuation was a strategic choice to exit an unprofitable product and refocus resources on SUBLOCADE, which posted record Q3 2026 net revenue of $267 million (+22% YoY) and drove overall company revenue up 13% to $356 million.
  • Indivior stated explicitly that the discontinuation was not related to any safety or efficacy issues with Perseris, and the company continues to benefit from its core opioid use disorder franchise.
  • The removal of Perseris selling costs and the 130-person headcount reduction improved the company's cost structure and operating margins ahead of the planned Supernus merger.
Bear case
  • The drug has been fully discontinued (availability ended May 31, 2026), reflecting a failed commercial launch. Indivior took a $85 million settlement with end-payor plaintiffs around the same period, and cut 130 jobs.
  • Perseris faced an intensely competitive long-acting injectable antipsychotic market (Janssen's Risperdal Consta, Otsuka's Abilify Maintena, and newer entrants) plus growing payer management pressure that made the product financially unviable.
  • The company's share price dropped ~34-40% on the July 2024 discontinuation announcement, and multiple securities class action lawsuits were filed alleging misleading statements about Perseris and Sublocade performance (though the class action was dismissed in August 2025).

Other drugs in filings and trials

no drug report yet
  • PERSERIS KIT Last: Approval · Jul 27, 2018
  • SUBLOCADE Last: Approval · Nov 30, 2017

Past FDA events & how the stock moved

3 events
DateDrugEvent1 day5 days
May 22, 2023OPVEEApproval−5.1%−6.2%
Jul 27, 2018PERSERIS KITApproval−1.1%−3.1%
Nov 30, 2017SUBLOCADEApproval+7.8%+1.0%

Clinical trials

1 Phase 2/3
DrugTrialPhaseStatusEnrolledPrimary completion
INDV-6001INDV-6001 Multiple-Dose Pharmacokinetic StudyPhase 2Completed123Jan 21, 2026