InMed Pharmaceuticals, Inc.
InMed Pharmaceuticals, Inc. Q4 FY2020 earnings call
September 8, 2020 · fiscal period ended 2020-06
EPS · actual vs est
Revenue · actual vs est
Summary
Generated 2020-09-08
Management highlights
- Therapeutic development: INM-755 Phase 1 trial advanced, second Phase 1 trial near enrollment completion; INM-088 for glaucoma in preclinical testing near formulation selection.
- Cannabinoid manufacturing: IntegraSyn platform developed, working on scale-up for GMP-batch production.
- General updates: Progress made despite COVID-19; clinical trial applications for INM-755 EB study delayed to Q1 2021; IntegraSyn GMP batch-ready delayed to Q1 2021; share consolidation completed; capital managed carefully with focus on R&D commitments.
Segment performance
InMed has therapeutic development programs and a cannabinoid manufacturing platform. The lead clinical program INM-755 advanced to the second Phase 1 clinical trial nearing enrollment completion. INM-088 for glaucoma is in preclinical testing near formulation selection. IntegraSyn, the cannabinoid manufacturing platform, is being scaled up for GMP-batch production. No specific revenue contribution percentages provided.
Guidance
- Anticipate Phase 1 trial results from INM-755 in Q4 2020.
- Clinical trial applications for INM-755 EB study now expected in Q1 2021, delayed from previous guidance.
- IntegraSyn GMP batch-ready now expected by end of Q1 2021, delayed from end of calendar 2020.
- Cash runway extended to at least Q3 2021 with cash management efforts.
Risks
- COVID-19 related restrictions impacting trial timelines and enrollment schedules.
- Protracted financing process due to regulatory delays, currently in a U.S. regulatory quiet period limiting comment on financing status.
Q&A highlights
Q: Changed timing for CTA filings for the EB trial, when might enrollment start?
A: Filings in Q1 2021, enrollment likely early in Q2.
Q: Status of INM-088 formulation decision?
A: Still evaluating, considering cost and economics of in-house vs external options.
Q: Pluses of the IntegraSyn process?
A: Cost efficiency, ability to mass produce enzyme for efficient cannabinoid production, and use of existing purification processes.
Q: Timeline for NASDAQ listing?
A: Ongoing, in regulatory quiet period, unable to speculate on exact timing but working diligently to move forward.
Q: Important patents?
A: Biosynthesis/IntegraSyn related patents and glaucoma neuroprotection patent are important; ongoing patent filings with expected allowances in near future.
Q: Status of INM-755 second Phase 1 trial?
A: Completing enrollment this week, COVID delays but center in Leiden helped keep on track.
Q: Importance of cannabinoid pharmaceuticals summit?
A: Important for advancing the field, combating misinformation about cannabinoids, and supporting pharmaceutical research development.
Key numbers
Reported versus consensus
Earnings calendar feed
| Metric | Reported | Consensus | Delta | Prior year |
|---|---|---|---|---|
| EPS | $-0.44 | $-0.66 | +33.3% | — |
| Revenue | — | — | — | — |
Transcript
September 8, 2020Full transcript unavailable for redistribution
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